Canonical Allele Identifier: CA645601251

Gene: RPS6KA3

Linked Data

• COSMIC: COSM1625776

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20172795_20172800del , CM000685.2:g.20172795_20172800del	GRCh38
NC_000023.10:g.20190913_20190918del , CM000685.1:g.20190913_20190918del	GRCh37
NC_000023.9:g.20100834_20100839del	NCBI36
NG_007488.1:g.98833_98838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.1299_1304del MANE Select	ENSP00000368884.3:p.Ser434_Val435del
ENST00000457145.6:c.1212_1217del	ENSP00000407655.2:p.Ser405_Val406del
ENST00000642835.1:c.1215_1220del	ENSP00000494769.1:p.Ser406_Val407del
ENST00000643073.1:c.917_922del	ENSP00000495839.1:n.917_922del
ENST00000643085.1:c.1215_1220del	ENSP00000496271.1:p.Ser406_Val407del
ENST00000643337.1:c.1215_1220del	ENSP00000493487.1:p.Ser406_Val407del
ENST00000643402.1:c.1215_1220del	ENSP00000493862.1:p.Ser406_Val407del
ENST00000644368.1:c.1215_1220del	ENSP00000495776.1:p.Ser406_Val407del
ENST00000644893.1:c.1212_1217del	ENSP00000495974.1:p.Ser405_Val406del
ENST00000645268.1:c.*520_*525del	ENSP00000496226.1:n.*520_*525del
ENST00000645270.1:c.1215_1220del	ENSP00000494967.1:p.Ser406_Val407del
ENST00000646610.1:c.1215_1220del	ENSP00000495462.1:p.Ser406_Val407del
ENST00000647265.1:c.1215_1220del	ENSP00000494220.1:p.Ser406_Val407del
ENST00000379565.7:c.1299_1304del	ENSP00000368884.3:p.Ser434_Val435del
ENST00000479809.1:n.65_70del
NM_004586.2:c.1299_1304del	NP_004577.1:p.Ser434_Val435del
XM_005274573.2:c.1296_1301del	XP_005274630.1:p.Ser433_Val434del
XM_005274577.2:c.1209_1214del	XP_005274634.1:p.Ser404_Val405del
XM_006724507.2:c.1212_1217del	XP_006724570.1:p.Ser405_Val406del
XM_011545555.1:c.1317_1322del	XP_011543857.1:p.Ser440_Val441del
XM_011545556.1:c.1314_1319del	XP_011543858.1:p.Ser439_Val440del
XM_011545557.1:c.1233_1238del	XP_011543859.1:p.Ser412_Val413del
XM_011545558.1:c.1233_1238del	XP_011543860.1:p.Ser412_Val413del
XM_011545559.1:c.1233_1238del	XP_011543861.1:p.Ser412_Val413del
XM_011545560.1:c.1233_1238del	XP_011543862.1:p.Ser412_Val413del
XM_011545561.1:c.1233_1238del	XP_011543863.1:p.Ser412_Val413del
XM_011545562.1:c.1230_1235del	XP_011543864.1:p.Ser411_Val412del
XM_011545563.1:c.1215_1220del	XP_011543865.1:p.Ser406_Val407del
XM_005274577.3:c.1209_1214del	XP_005274634.1:p.Ser404_Val405del
XM_006724507.3:c.1212_1217del	XP_006724570.1:p.Ser405_Val406del
XM_011545557.2:c.1233_1238del	XP_011543859.1:p.Ser412_Val413del
XM_011545558.2:c.1233_1238del	XP_011543860.1:p.Ser412_Val413del
XM_011545561.2:c.1233_1238del	XP_011543863.1:p.Ser412_Val413del
XM_011545562.2:c.1230_1235del	XP_011543864.1:p.Ser411_Val412del
XM_011545563.3:c.1215_1220del	XP_011543865.1:p.Ser406_Val407del
XM_017029713.1:c.1215_1220del	XP_016885202.1:p.Ser406_Val407del
XM_017029714.2:c.1215_1220del	XP_016885203.1:p.Ser406_Val407del
XM_017029715.2:c.1215_1220del	XP_016885204.1:p.Ser406_Val407del
XM_017029716.1:c.1215_1220del	XP_016885205.1:p.Ser406_Val407del
XM_017029717.2:c.1215_1220del	XP_016885206.1:p.Ser406_Val407del
XM_017029718.2:c.1212_1217del	XP_016885207.1:p.Ser405_Val406del
XM_017029719.2:c.1212_1217del	XP_016885208.1:p.Ser405_Val406del
NM_004586.3:c.1299_1304del MANE Select	NP_004577.1:p.Ser434_Val435del