Canonical Allele Identifier: CA891837233

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965329_87965331delinsGCT , CM000672.2:g.87965329_87965331delinsGCT	GRCh38
NC_000010.10:g.89725086_89725088delinsGCT , CM000672.1:g.89725086_89725088delinsGCT	GRCh37
NC_000010.9:g.89715066_89715068delinsGCT	NCBI36
NG_007466.2:g.106891_106893delinsGCT , LRG_311:g.106891_106893delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1162_1164delinsGCT	ENSP00000514759.2:p.Pro388Ala
ENST00000710265.1:c.*98_*100delinsGCT	ENSP00000518161.1:n.*98_*100delinsGCT
ENST00000688158.2:n.1804_1806delinsGCT
ENST00000688922.2:c.*899_*901delinsGCT	ENSP00000508742.2:n.*899_*901delinsGCT
ENST00000700021.1:c.1024_1026delinsGCT	ENSP00000514757.1:p.Pro342Ala
ENST00000700022.1:c.*408_*410delinsGCT	ENSP00000514758.1:n.*408_*410delinsGCT
ENST00000700023.1:n.2227_2229delinsGCT
ENST00000700024.1:n.2461_2463delinsGCT
ENST00000706954.1:c.1069_1071delinsGCT	ENSP00000516674.1:p.Pro357Ala
ENST00000706955.1:c.*1104_*1106delinsGCT	ENSP00000516675.1:n.*1104_*1106delinsGCT
ENST00000686459.1:c.*655_*657delinsGCT	ENSP00000508909.1:n.*655_*657delinsGCT
ENST00000688158.1:c.*1180_*1182delinsGCT	ENSP00000509254.1:n.*1180_*1182delinsGCT
ENST00000688308.1:c.1069_1071delinsGCT	ENSP00000508752.1:p.Pro357Ala
ENST00000688922.1:c.990_992delinsGCT
ENST00000693560.1:c.1588_1590delinsGCT	ENSP00000509861.1:p.Pro530Ala
ENST00000371953.8:c.1069_1071delinsGCT MANE Select	ENSP00000361021.3:p.Pro357Ala
ENST00000371953.7:c.1069_1071delinsGCT	ENSP00000361021.3:p.Pro357Ala
NM_000314.5:c.1069_1071delinsGCT	NP_000305.3:p.Pro357Ala
NM_000314.6:c.1069_1071delinsGCT	NP_000305.3:p.Pro357Ala
NM_001304717.2:c.1588_1590delinsGCT	NP_001291646.2:p.Pro530Ala
NM_001304718.1:c.478_480delinsGCT	NP_001291647.1:p.Pro160Ala
XM_006717926.2:c.1024_1026delinsGCT	XP_006717989.1:p.Pro342Ala
XM_011539982.1:c.973_975delinsGCT	XP_011538284.1:p.Pro325Ala
XR_945791.1:n.1639_1641delinsGCT
NM_000314.7:c.1069_1071delinsGCT	NP_000305.3:p.Pro357Ala
NM_001304717.5:c.1588_1590delinsGCT	NP_001291646.4:p.Pro530Ala
NM_001304718.2:c.478_480delinsGCT	NP_001291647.1:p.Pro160Ala
NM_000314.8:c.1069_1071delinsGCT MANE Select	NP_000305.3:p.Pro357Ala