Canonical Allele Identifier: CA891838740

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952142_87952144delinsGCT , CM000672.2:g.87952142_87952144delinsGCT	GRCh38
NC_000010.10:g.89711899_89711901delinsGCT , CM000672.1:g.89711899_89711901delinsGCT	GRCh37
NC_000010.9:g.89701879_89701881delinsGCT	NCBI36
NG_007466.2:g.93704_93706delinsGCT , LRG_311:g.93704_93706delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.517_519delinsGCT	ENSP00000514759.2:p.Arg173Ala
ENST00000710265.1:c.517_519delinsGCT	ENSP00000518161.1:p.Arg173Ala
ENST00000472832.3:c.517_519delinsGCT	ENSP00000483066.2:p.Arg173Ala
ENST00000688158.2:n.1252_1254delinsGCT
ENST00000688922.2:c.*347_*349delinsGCT	ENSP00000508742.2:n.*347_*349delinsGCT
ENST00000700021.1:c.472_474delinsGCT	ENSP00000514757.1:p.Arg158Ala
ENST00000700022.1:c.493-5711_493-5709delinsGCT	ENSP00000514758.1:n.493-5711_493-5709delinsGCT
ENST00000700023.1:n.1675_1677delinsGCT
ENST00000700024.1:n.1909_1911delinsGCT
ENST00000700025.1:n.1286_1288delinsGCT
ENST00000700029.1:c.351_353delinsGCT
ENST00000706954.1:c.517_519delinsGCT	ENSP00000516674.1:p.Arg173Ala
ENST00000706955.1:c.*552_*554delinsGCT	ENSP00000516675.1:n.*552_*554delinsGCT
ENST00000686459.1:c.*103_*105delinsGCT	ENSP00000508909.1:n.*103_*105delinsGCT
ENST00000688158.1:c.*628_*630delinsGCT	ENSP00000509254.1:n.*628_*630delinsGCT
ENST00000688308.1:c.517_519delinsGCT	ENSP00000508752.1:p.Arg173Ala
ENST00000688922.1:c.438_440delinsGCT
ENST00000693560.1:c.1036_1038delinsGCT	ENSP00000509861.1:p.Arg346Ala
ENST00000371953.8:c.517_519delinsGCT MANE Select	ENSP00000361021.3:p.Arg173Ala
ENST00000371953.7:c.517_519delinsGCT	ENSP00000361021.3:p.Arg173Ala
NM_000314.5:c.517_519delinsGCT	NP_000305.3:p.Arg173Ala
NM_000314.6:c.517_519delinsGCT	NP_000305.3:p.Arg173Ala
NM_001304717.2:c.1036_1038delinsGCT	NP_001291646.2:p.Arg346Ala
NM_001304718.1:c.-75_-73delinsGCT	NP_001291647.1:n.-75_-73delinsGCT
XM_006717926.2:c.472_474delinsGCT	XP_006717989.1:p.Arg158Ala
XM_011539981.1:c.517_519delinsGCT	XP_011538283.1:p.Arg173Ala
XM_011539982.1:c.421_423delinsGCT	XP_011538284.1:p.Arg141Ala
XR_945789.1:n.1388_1390delinsGCT
XR_945790.1:n.1505_1507delinsGCT
XR_945791.1:n.1205-5711_1205-5709delinsGCT
NM_000314.7:c.517_519delinsGCT	NP_000305.3:p.Arg173Ala
NM_001304717.5:c.1036_1038delinsGCT	NP_001291646.4:p.Arg346Ala
NM_001304718.2:c.-75_-73delinsGCT	NP_001291647.1:n.-75_-73delinsGCT
NM_000314.8:c.517_519delinsGCT MANE Select	NP_000305.3:p.Arg173Ala