Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.29197585T>A	CA346466007	ALK,CLIP4	c.579T>A (n.579T>A) c.4030A>T (p.Ser1344Cys) c.1257A>T n.907A>T c.826A>T (p.Ser276Cys) c.910A>T (p.Ser304Cys) c.2899A>T (p.Ser967Cys) c.1183A>T (p.Ser395Cys)
2	g.29197585T>C	CA1593701	ALK,CLIP4	c.579T>C (n.579T>C) c.4030A>G (p.Ser1344Gly) c.1257A>G n.907A>G c.826A>G (p.Ser276Gly) c.910A>G (p.Ser304Gly) c.2899A>G (p.Ser967Gly) c.1183A>G (p.Ser395Gly)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.29197585T>G	CA346466011	ALK,CLIP4	c.579T>G (n.579T>G) c.4030A>C (p.Ser1344Arg) c.1257A>C n.907A>C c.826A>C (p.Ser276Arg) c.910A>C (p.Ser304Arg) c.2899A>C (p.Ser967Arg) c.1183A>C (p.Ser395Arg)
2	g.29197585T=	CA1241075331	ALK,CLIP4	c.579T= (n.579T=) c.4030A= (p.Ser1344=) c.1257A= n.907A= c.826A= (p.Ser276=) c.910A= (p.Ser304=) c.2899A= (p.Ser967=) c.1183A= (p.Ser395=)
2	g.29197586G>A	CA425433902	ALK,CLIP4	c.580G>A (n.580G>A) c.4029C>T (p.Thr1343=) c.1256C>T n.906C>T c.825C>T (p.Thr275=) c.909C>T (p.Thr303=) c.2898C>T (p.Thr966=) c.1182C>T (p.Thr394=)	dbSNP
2	g.29197586G>C	CA425433904	ALK,CLIP4	c.580G>C (n.580G>C) c.4029C>G (p.Thr1343=) c.1256C>G n.906C>G c.825C>G (p.Thr275=) c.909C>G (p.Thr303=) c.2898C>G (p.Thr966=) c.1182C>G (p.Thr394=)	ClinVar dbSNP
2	g.29197586G>T	CA425433903	ALK,CLIP4	c.580G>T (n.580G>T) c.4029C>A (p.Thr1343=) c.1256C>A n.906C>A c.825C>A (p.Thr275=) c.909C>A (p.Thr303=) c.2898C>A (p.Thr966=) c.1182C>A (p.Thr394=)	dbSNP gnomAD v4
2	g.29197587G>A	CA1593702	ALK,CLIP4	c.581G>A (n.581G>A) c.4028C>T (p.Thr1343Ile) c.1255C>T n.905C>T c.824C>T (p.Thr275Ile) c.908C>T (p.Thr303Ile) c.2897C>T (p.Thr966Ile) c.1181C>T (p.Thr394Ile)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.29197587G>C	CA346466015	ALK,CLIP4	c.581G>C (n.581G>C) c.4028C>G (p.Thr1343Ser) c.1255C>G n.905C>G c.824C>G (p.Thr275Ser) c.908C>G (p.Thr303Ser) c.2897C>G (p.Thr966Ser) c.1181C>G (p.Thr394Ser)	ClinVar dbSNP gnomAD v3 gnomAD v4
2	g.29197587G=	CA1241075332	ALK,CLIP4	c.581G= (n.581G=) c.4028C= (p.Thr1343=) c.1255C= n.905C= c.824C= (p.Thr275=) c.908C= (p.Thr303=) c.2897C= (p.Thr966=) c.1181C= (p.Thr394=)
2	g.29197587G>T	CA346466017	ALK,CLIP4	c.581G>T (n.581G>T) c.4028C>A (p.Thr1343Asn) c.1255C>A n.905C>A c.824C>A (p.Thr275Asn) c.908C>A (p.Thr303Asn) c.2897C>A (p.Thr966Asn) c.1181C>A (p.Thr394Asn)	dbSNP
2	g.29197588T>A	CA346466020	ALK,CLIP4	c.582T>A (n.582T>A) c.4027A>T (p.Thr1343Ser) c.1254A>T n.904A>T c.823A>T (p.Thr275Ser) c.907A>T (p.Thr303Ser) c.2896A>T (p.Thr966Ser) c.1180A>T (p.Thr394Ser)	dbSNP
2	g.29197588T>C	CA346466022	ALK,CLIP4	c.582T>C (n.582T>C) c.4027A>G (p.Thr1343Ala) c.1254A>G n.904A>G c.823A>G (p.Thr275Ala) c.907A>G (p.Thr303Ala) c.2896A>G (p.Thr966Ala) c.1180A>G (p.Thr394Ala)	dbSNP
2	g.29197588T>G	CA346466025	ALK,CLIP4	c.582T>G (n.582T>G) c.4027A>C (p.Thr1343Pro) c.1254A>C n.904A>C c.823A>C (p.Thr275Pro) c.907A>C (p.Thr303Pro) c.2896A>C (p.Thr966Pro) c.1180A>C (p.Thr394Pro)	dbSNP
2	g.29197589G>A	CA425433905	ALK,CLIP4	c.583G>A (n.583G>A) c.4026C>T (p.Val1342=) c.1253C>T n.903C>T c.822C>T (p.Val274=) c.906C>T (p.Val302=) c.2895C>T (p.Val965=) c.1179C>T (p.Val393=)	ClinVar dbSNP
2	g.29197589G>C	CA425433906	ALK,CLIP4	c.583G>C (n.583G>C) c.4026C>G (p.Val1342=) c.1253C>G n.903C>G c.822C>G (p.Val274=) c.906C>G (p.Val302=) c.2895C>G (p.Val965=) c.1179C>G (p.Val393=)	dbSNP
2	g.29197589G>T	CA425433907	ALK,CLIP4	c.583G>T (n.583G>T) c.4026C>A (p.Val1342=) c.1253C>A n.903C>A c.822C>A (p.Val274=) c.906C>A (p.Val302=) c.2895C>A (p.Val965=) c.1179C>A (p.Val393=)
2	g.29197590A>C	CA346466027	ALK,CLIP4	c.584A>C (n.584A>C) c.4025T>G (p.Val1342Gly) c.1252T>G n.902T>G c.821T>G (p.Val274Gly) c.905T>G (p.Val302Gly) c.2894T>G (p.Val965Gly) c.1178T>G (p.Val393Gly)	dbSNP
2	g.29197590A>G	CA346466030	ALK,CLIP4	c.584A>G (n.584A>G) c.4025T>C (p.Val1342Ala) c.1252T>C n.902T>C c.821T>C (p.Val274Ala) c.905T>C (p.Val302Ala) c.2894T>C (p.Val965Ala) c.1178T>C (p.Val393Ala)	dbSNP
2	g.29197590A>T	CA346466032	ALK,CLIP4	c.584A>T (n.584A>T) c.4025T>A (p.Val1342Asp) c.1252T>A n.902T>A c.821T>A (p.Val274Asp) c.905T>A (p.Val302Asp) c.2894T>A (p.Val965Asp) c.1178T>A (p.Val393Asp)	ClinVar dbSNP
2	g.29197591C>A	CA346466038	ALK,CLIP4	c.585C>A (n.585C>A) c.4024G>T (p.Val1342Phe) c.1251G>T n.901G>T c.820G>T (p.Val274Phe) c.904G>T (p.Val302Phe) c.2893G>T (p.Val965Phe) c.1177G>T (p.Val393Phe)
2	g.29197591C=	CA1241075333	ALK,CLIP4	c.585C= (n.585C=) c.4024G= (p.Val1342=) c.1251G= n.901G= c.820G= (p.Val274=) c.904G= (p.Val302=) c.2893G= (p.Val965=) c.1177G= (p.Val393=)
2	g.29197591C>G	CA346466036	ALK,CLIP4	c.585C>G (n.585C>G) c.4024G>C (p.Val1342Leu) c.1251G>C n.901G>C c.820G>C (p.Val274Leu) c.904G>C (p.Val302Leu) c.2893G>C (p.Val965Leu) c.1177G>C (p.Val393Leu)
2	g.29197591C>T	CA1593703	ALK,CLIP4	c.585C>T (n.585C>T) c.4024G>A (p.Val1342Ile) c.1251G>A n.901G>A c.820G>A (p.Val274Ile) c.904G>A (p.Val302Ile) c.2893G>A (p.Val965Ile) c.1177G>A (p.Val393Ile)	dbSNP ExAC gnomAD v2 gnomAD v4
2	g.29197592A>C	CA346466040	ALK,CLIP4	c.586A>C (n.586A>C) c.4023T>G (p.Phe1341Leu) c.1250T>G n.900T>G c.819T>G (p.Phe273Leu) c.903T>G (p.Phe301Leu) c.2892T>G (p.Phe964Leu) c.1176T>G (p.Phe392Leu)
2	g.29197592A>G	CA425433908	ALK,CLIP4	c.586A>G (n.586A>G) c.4023T>C (p.Phe1341=) c.1250T>C n.900T>C c.819T>C (p.Phe273=) c.903T>C (p.Phe301=) c.2892T>C (p.Phe964=) c.1176T>C (p.Phe392=)	ClinVar
2	g.29197592A>T	CA346466043	ALK,CLIP4	c.586A>T (n.586A>T) c.4023T>A (p.Phe1341Leu) c.1250T>A n.900T>A c.819T>A (p.Phe273Leu) c.903T>A (p.Phe301Leu) c.2892T>A (p.Phe964Leu) c.1176T>A (p.Phe392Leu)	dbSNP
2	g.29197593_29197594del	CA2580066451	ALK,CLIP4	c.587_588del (n.587_588del) c.4022_4023del (p.Phe1341CysfsTer30) c.1249_1250del n.899_900del c.818_819del (p.Phe273CysfsTer30) c.902_903del (p.Phe301CysfsTer30) c.2891_2892del (p.Phe964CysfsTer30) c.1175_1176del (p.Phe392CysfsTer30)	ClinVar
2	g.29197593A>C	CA346466045	ALK,CLIP4	c.587A>C (n.587A>C) c.4022T>G (p.Phe1341Cys) c.1249T>G n.899T>G c.818T>G (p.Phe273Cys) c.902T>G (p.Phe301Cys) c.2891T>G (p.Phe964Cys) c.1175T>G (p.Phe392Cys)
2	g.29197593A>G	CA346466047	ALK,CLIP4	c.587A>G (n.587A>G) c.4022T>C (p.Phe1341Ser) c.1249T>C n.899T>C c.818T>C (p.Phe273Ser) c.902T>C (p.Phe301Ser) c.2891T>C (p.Phe964Ser) c.1175T>C (p.Phe392Ser)	dbSNP COSMIC
2	g.29197593A>T	CA346466048	ALK,CLIP4	c.587A>T (n.587A>T) c.4022T>A (p.Phe1341Tyr) c.1249T>A n.899T>A c.818T>A (p.Phe273Tyr) c.902T>A (p.Phe301Tyr) c.2891T>A (p.Phe964Tyr) c.1175T>A (p.Phe392Tyr)	dbSNP
2	g.29197594A>C	CA346466051	ALK,CLIP4	c.588A>C (n.588A>C) c.4021T>G (p.Phe1341Val) c.1248T>G n.898T>G c.817T>G (p.Phe273Val) c.901T>G (p.Phe301Val) c.2890T>G (p.Phe964Val) c.1174T>G (p.Phe392Val)	dbSNP
2	g.29197594A>G	CA346466053	ALK,CLIP4	c.588A>G (n.588A>G) c.4021T>C (p.Phe1341Leu) c.1248T>C n.898T>C c.817T>C (p.Phe273Leu) c.901T>C (p.Phe301Leu) c.2890T>C (p.Phe964Leu) c.1174T>C (p.Phe392Leu)	dbSNP
2	g.29197594A>T	CA346466054	ALK,CLIP4	c.588A>T (n.588A>T) c.4021T>A (p.Phe1341Ile) c.1248T>A n.898T>A c.817T>A (p.Phe273Ile) c.901T>A (p.Phe301Ile) c.2890T>A (p.Phe964Ile) c.1174T>A (p.Phe392Ile)	dbSNP
2	g.29197595C>A	CA346466055	ALK,CLIP4	c.589C>A (n.589C>A) c.4020G>T (p.Glu1340Asp) c.1247G>T n.897G>T c.816G>T (p.Glu272Asp) c.900G>T (p.Glu300Asp) c.2889G>T (p.Glu963Asp) c.1173G>T (p.Glu391Asp)	dbSNP
2	g.29197595C>G	CA346466056	ALK,CLIP4	c.589C>G (n.589C>G) c.4020G>C (p.Glu1340Asp) c.1247G>C n.897G>C c.816G>C (p.Glu272Asp) c.900G>C (p.Glu300Asp) c.2889G>C (p.Glu963Asp) c.1173G>C (p.Glu391Asp)	dbSNP
2	g.29197595C>T	CA425433909	ALK,CLIP4	c.589C>T (n.589C>T) c.4020G>A (p.Glu1340=) c.1247G>A n.897G>A c.816G>A (p.Glu272=) c.900G>A (p.Glu300=) c.2889G>A (p.Glu963=) c.1173G>A (p.Glu391=)	ClinVar dbSNP
2	g.29197596T>A	CA346466059	ALK,CLIP4	c.590T>A (n.590T>A) c.4019A>T (p.Glu1340Val) c.1246A>T n.896A>T c.815A>T (p.Glu272Val) c.899A>T (p.Glu300Val) c.2888A>T (p.Glu963Val) c.1172A>T (p.Glu391Val)	COSMIC
2	g.29197596T>C	CA346466061	ALK,CLIP4	c.590T>C (n.590T>C) c.4019A>G (p.Glu1340Gly) c.1246A>G n.896A>G c.815A>G (p.Glu272Gly) c.899A>G (p.Glu300Gly) c.2888A>G (p.Glu963Gly) c.1172A>G (p.Glu391Gly)	ClinVar dbSNP gnomAD v4
2	g.29197596T>G	CA346466063	ALK,CLIP4	c.590T>G (n.590T>G) c.4019A>C (p.Glu1340Ala) c.1246A>C n.896A>C c.815A>C (p.Glu272Ala) c.899A>C (p.Glu300Ala) c.2888A>C (p.Glu963Ala) c.1172A>C (p.Glu391Ala)
2	g.29197596T=	CA1241075335	ALK,CLIP4	c.590T= (n.590T=) c.4019A= (p.Glu1340=) c.1246A= n.896A= c.815A= (p.Glu272=) c.899A= (p.Glu300=) c.2888A= (p.Glu963=) c.1172A= (p.Glu391=)
2	g.29197597C>A	CA346466067	ALK,CLIP4	c.591C>A (n.591C>A) c.4018G>T (p.Glu1340Ter) c.1245G>T n.895G>T c.814G>T (p.Glu272Ter) c.898G>T (p.Glu300Ter) c.2887G>T (p.Glu963Ter) c.1171G>T (p.Glu391Ter)
2	g.29197597C>G	CA346466070	ALK,CLIP4	c.591C>G (n.591C>G) c.4018G>C (p.Glu1340Gln) c.1245G>C n.895G>C c.814G>C (p.Glu272Gln) c.898G>C (p.Glu300Gln) c.2887G>C (p.Glu963Gln) c.1171G>C (p.Glu391Gln)
2	g.29197597C>T	CA346466065	ALK,CLIP4	c.591C>T (n.591C>T) c.4018G>A (p.Glu1340Lys) c.1245G>A n.895G>A c.814G>A (p.Glu272Lys) c.898G>A (p.Glu300Lys) c.2887G>A (p.Glu963Lys) c.1171G>A (p.Glu391Lys)
2	g.29197598C>A	CA425433910	ALK,CLIP4	c.592C>A (n.592C>A) c.4017G>T (p.Leu1339=) c.1244G>T n.894G>T c.813G>T (p.Leu271=) c.897G>T (p.Leu299=) c.2886G>T (p.Leu962=) c.1170G>T (p.Leu390=)	dbSNP
2	g.29197598C=	CA1241075338	ALK,CLIP4	c.592C= (n.592C=) c.4017G= (p.Leu1339=) c.1244G= n.894G= c.813G= (p.Leu271=) c.897G= (p.Leu299=) c.2886G= (p.Leu962=) c.1170G= (p.Leu390=)
2	g.29197598C>G	CA425433911	ALK,CLIP4	c.592C>G (n.592C>G) c.4017G>C (p.Leu1339=) c.1244G>C n.894G>C c.813G>C (p.Leu271=) c.897G>C (p.Leu299=) c.2886G>C (p.Leu962=) c.1170G>C (p.Leu390=)	dbSNP
2	g.29197598C>T	CA425433912	ALK,CLIP4	c.592C>T (n.592C>T) c.4017G>A (p.Leu1339=) c.1244G>A n.894G>A c.813G>A (p.Leu271=) c.897G>A (p.Leu299=) c.2886G>A (p.Leu962=) c.1170G>A (p.Leu390=)	ClinVar dbSNP gnomAD v4
2	g.29197599A=	CA1241075343	ALK,CLIP4	c.593A= (n.593A=) c.4016T= (p.Leu1339=) c.1243T= n.893T= c.812T= (p.Leu271=) c.896T= (p.Leu299=) c.2885T= (p.Leu962=) c.1169T= (p.Leu390=)
2	g.29197599A>C	CA346466074	ALK,CLIP4	c.593A>C (n.593A>C) c.4016T>G (p.Leu1339Arg) c.1243T>G n.893T>G c.812T>G (p.Leu271Arg) c.896T>G (p.Leu299Arg) c.2885T>G (p.Leu962Arg) c.1169T>G (p.Leu390Arg)

Number of alleles fetched