Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.29227061G>ACA1594122ALKc.2928C>T (p.His976=)
c.94C>T
c.1797C>T (p.His599=)
c.81C>T (p.His27=)
n.3784C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.29227061G>CCA346468094ALKc.2928C>G (p.His976Gln)
c.94C>G
c.1797C>G (p.His599Gln)
c.81C>G (p.His27Gln)
n.3784C>G
 dbSNP
2g.29227061G=CA1241092888ALKc.2928C= (p.His976=)
c.94C=
c.1797C= (p.His599=)
c.81C= (p.His27=)
n.3784C=
2g.29227061G>TCA346468095ALKc.2928C>A (p.His976Gln)
c.94C>A
c.1797C>A (p.His599Gln)
c.81C>A (p.His27Gln)
n.3784C>A
 ClinVar
2g.29227062T>ACA346468097ALKc.2927A>T (p.His976Leu)
c.93A>T
c.1796A>T (p.His599Leu)
c.80A>T (p.His27Leu)
n.3783A>T
2g.29227062T>CCA346468098ALKc.2927A>G (p.His976Arg)
c.93A>G
c.1796A>G (p.His599Arg)
c.80A>G (p.His27Arg)
n.3783A>G
2g.29227062T>GCA346468101ALKc.2927A>C (p.His976Pro)
c.93A>C
c.1796A>C (p.His599Pro)
c.80A>C (p.His27Pro)
n.3783A>C
 gnomAD v4
2g.29227063G>ACA346468104ALKc.2926C>T (p.His976Tyr)
c.92C>T
c.1795C>T (p.His599Tyr)
c.79C>T (p.His27Tyr)
n.3782C>T
 ClinVar dbSNP
2g.29227063G>CCA346468106ALKc.2926C>G (p.His976Asp)
c.92C>G
c.1795C>G (p.His599Asp)
c.79C>G (p.His27Asp)
n.3782C>G
 dbSNP
2g.29227063G=CA1241092889ALKc.2926C= (p.His976=)
c.92C=
c.1795C= (p.His599=)
c.79C= (p.His27=)
n.3782C=
2g.29227063G>TCA346468108ALKc.2926C>A (p.His976Asn)
c.92C>A
c.1795C>A (p.His599Asn)
c.79C>A (p.His27Asn)
n.3782C>A
2g.29227064G>ACA425436029ALKc.2925C>T (p.Gly975=)
c.91C>T
c.1794C>T (p.Gly598=)
c.78C>T (p.Gly26=)
n.3781C>T
2g.29227064G>CCA425436030ALKc.2925C>G (p.Gly975=)
c.91C>G
c.1794C>G (p.Gly598=)
c.78C>G (p.Gly26=)
n.3781C>G
2g.29227064G>TCA425436031ALKc.2925C>A (p.Gly975=)
c.91C>A
c.1794C>A (p.Gly598=)
c.78C>A (p.Gly26=)
n.3781C>A
2g.29227065C>ACA346468115ALKc.2924G>T (p.Gly975Val)
c.90G>T
c.1793G>T (p.Gly598Val)
c.77G>T (p.Gly26Val)
n.3780G>T
 ClinVar dbSNP gnomAD v4
2g.29227065C=CA1241092890ALKc.2924G= (p.Gly975=)
c.90G=
c.1793G= (p.Gly598=)
c.77G= (p.Gly26=)
n.3780G=
2g.29227065C>GCA346468110ALKc.2924G>C (p.Gly975Ala)
c.90G>C
c.1793G>C (p.Gly598Ala)
c.77G>C (p.Gly26Ala)
n.3780G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.29227065C>TCA346468113ALKc.2924G>A (p.Gly975Asp)
c.90G>A
c.1793G>A (p.Gly598Asp)
c.77G>A (p.Gly26Asp)
n.3780G>A
 dbSNP gnomAD v4
2g.29227066C>ACA346468117ALKc.2923G>T (p.Gly975Cys)
c.89G>T
c.1792G>T (p.Gly598Cys)
c.76G>T (p.Gly26Cys)
n.3779G>T
 dbSNP
2g.29227066C>GCA346468121ALKc.2923G>C (p.Gly975Arg)
c.89G>C
c.1792G>C (p.Gly598Arg)
c.76G>C (p.Gly26Arg)
n.3779G>C
 dbSNP
2g.29227066C>TCA346468123ALKc.2923G>A (p.Gly975Ser)
c.89G>A
c.1792G>A (p.Gly598Ser)
c.76G>A (p.Gly26Ser)
n.3779G>A
 dbSNP
2g.29227067T>ACA346468124ALKc.2922A>T (p.Glu974Asp)
c.88A>T
c.1791A>T (p.Glu597Asp)
c.75A>T (p.Glu25Asp)
n.3778A>T
2g.29227067T>CCA425436034ALKc.2922A>G (p.Glu974=)
c.88A>G
c.1791A>G (p.Glu597=)
c.75A>G (p.Glu25=)
n.3778A>G
 dbSNP
2g.29227067T>GCA346468125ALKc.2922A>C (p.Glu974Asp)
c.88A>C
c.1791A>C (p.Glu597Asp)
c.75A>C (p.Glu25Asp)
n.3778A>C
 ClinVar
2g.29227068delCA2658460478ALKc.2922del (p.Gly975AlafsTer5)
c.88del
c.1791del (p.Gly598AlafsTer5)
c.75del (p.Gly26AlafsTer5)
n.3778del
 gnomAD v4
2g.29227068T>ACA346468129ALKc.2921A>T (p.Glu974Val)
c.87A>T
c.1790A>T (p.Glu597Val)
c.74A>T (p.Glu25Val)
n.3777A>T
2g.29227068T>CCA346468130ALKc.2921A>G (p.Glu974Gly)
c.87A>G
c.1790A>G (p.Glu597Gly)
c.74A>G (p.Glu25Gly)
n.3777A>G
2g.29227068T>GCA346468132ALKc.2921A>C (p.Glu974Ala)
c.87A>C
c.1790A>C (p.Glu597Ala)
c.74A>C (p.Glu25Ala)
n.3777A>C
2g.29227069C>ACA346468133ALKc.2920G>T (p.Glu974Ter)
c.86G>T
c.1789G>T (p.Glu597Ter)
c.73G>T (p.Glu25Ter)
n.3776G>T
 dbSNP
2g.29227069C>GCA346468135ALKc.2920G>C (p.Glu974Gln)
c.86G>C
c.1789G>C (p.Glu597Gln)
c.73G>C (p.Glu25Gln)
n.3776G>C
 dbSNP
2g.29227069C>TCA346468136ALKc.2920G>A (p.Glu974Lys)
c.86G>A
c.1789G>A (p.Glu597Lys)
c.73G>A (p.Glu25Lys)
n.3776G>A
 dbSNP
2g.29227070C>ACA346468139ALKc.2919G>T (p.Met973Ile)
c.85G>T
c.1788G>T (p.Met596Ile)
c.72G>T (p.Met24Ile)
n.3775G>T
 dbSNP
2g.29227070C>GCA346468138ALKc.2919G>C (p.Met973Ile)
c.85G>C
c.1788G>C (p.Met596Ile)
c.72G>C (p.Met24Ile)
n.3775G>C
2g.29227070C>TCA346468137ALKc.2919G>A (p.Met973Ile)
c.85G>A
c.1788G>A (p.Met596Ile)
c.72G>A (p.Met24Ile)
n.3775G>A
 ClinVar dbSNP
2g.29227071A>CCA346468141ALKc.2918T>G (p.Met973Arg)
c.84T>G
c.1787T>G (p.Met596Arg)
c.71T>G (p.Met24Arg)
n.3774T>G
 dbSNP
2g.29227071A>GCA346468140ALKc.2918T>C (p.Met973Thr)
c.84T>C
c.1787T>C (p.Met596Thr)
c.71T>C (p.Met24Thr)
n.3774T>C
2g.29227071A>TCA346468144ALKc.2918T>A (p.Met973Lys)
c.84T>A
c.1787T>A (p.Met596Lys)
c.71T>A (p.Met24Lys)
n.3774T>A
 dbSNP
2g.29227072T>ACA346468146ALKc.2917A>T (p.Met973Leu)
c.83A>T
c.1786A>T (p.Met596Leu)
c.70A>T (p.Met24Leu)
n.3773A>T
2g.29227072T>CCA346468148ALKc.2917A>G (p.Met973Val)
c.83A>G
c.1786A>G (p.Met596Val)
c.70A>G (p.Met24Val)
n.3773A>G
 ClinVar dbSNP
2g.29227072T>GCA346468150ALKc.2917A>C (p.Met973Leu)
c.83A>C
c.1786A>C (p.Met596Leu)
c.70A>C (p.Met24Leu)
n.3773A>C
2g.29227072T=CA1241092891ALKc.2917A= (p.Met973=)
c.83A=
c.1786A= (p.Met596=)
c.70A= (p.Met24=)
n.3773A=
2g.29227073C>ACA425436037ALKc.2916G>T (p.Val972=)
c.82G>T
c.1785G>T (p.Val595=)
c.69G>T (p.Val23=)
n.3772G>T
 dbSNP
2g.29227073C>GCA425436038ALKc.2916G>C (p.Val972=)
c.82G>C
c.1785G>C (p.Val595=)
c.69G>C (p.Val23=)
n.3772G>C
 dbSNP
2g.29227073C>TCA425436040ALKc.2916G>A (p.Val972=)
c.82G>A
c.1785G>A (p.Val595=)
c.69G>A (p.Val23=)
n.3772G>A
 dbSNP gnomAD v4
2g.29227074A=CA1241092892ALKc.2915T= (p.Val972=)
c.81T=
c.1784T= (p.Val595=)
c.68T= (p.Val23=)
n.3771T=
2g.29227074A>CCA346468153ALKc.2915T>G (p.Val972Gly)
c.81T>G
c.1784T>G (p.Val595Gly)
c.68T>G (p.Val23Gly)
n.3771T>G
2g.29227074A>GCA346468155ALKc.2915T>C (p.Val972Ala)
c.81T>C
c.1784T>C (p.Val595Ala)
c.68T>C (p.Val23Ala)
n.3771T>C
 ClinVar dbSNP gnomAD v4
2g.29227074A>TCA346468158ALKc.2915T>A (p.Val972Glu)
c.81T>A
c.1784T>A (p.Val595Glu)
c.68T>A (p.Val23Glu)
n.3771T>A
 dbSNP
2g.29227075C>ACA346468160ALKc.2915-1G>T (n.2915-1G>T)
c.81-1G>T
c.1784-1G>T (n.1784-1G>T)
c.68-1G>T (n.68-1G>T)
n.3771-1G>T
 dbSNP
2g.29227075C>GCA346468161ALKc.2915-1G>C (n.2915-1G>C)
c.81-1G>C
c.1784-1G>C (n.1784-1G>C)
c.68-1G>C (n.68-1G>C)
n.3771-1G>C
 dbSNP

Number of alleles fetched