Canonical Allele Identifier: CA891837226

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965329_87965331delinsAAT , CM000672.2:g.87965329_87965331delinsAAT	GRCh38
NC_000010.10:g.89725086_89725088delinsAAT , CM000672.1:g.89725086_89725088delinsAAT	GRCh37
NC_000010.9:g.89715066_89715068delinsAAT	NCBI36
NG_007466.2:g.106891_106893delinsAAT , LRG_311:g.106891_106893delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1162_1164delinsAAT	ENSP00000514759.2:p.Pro388Asn
ENST00000710265.1:c.*98_*100delinsAAT	ENSP00000518161.1:n.*98_*100delinsAAT
ENST00000688158.2:n.1804_1806delinsAAT
ENST00000688922.2:c.*899_*901delinsAAT	ENSP00000508742.2:n.*899_*901delinsAAT
ENST00000700021.1:c.1024_1026delinsAAT	ENSP00000514757.1:p.Pro342Asn
ENST00000700022.1:c.*408_*410delinsAAT	ENSP00000514758.1:n.*408_*410delinsAAT
ENST00000700023.1:n.2227_2229delinsAAT
ENST00000700024.1:n.2461_2463delinsAAT
ENST00000706954.1:c.1069_1071delinsAAT	ENSP00000516674.1:p.Pro357Asn
ENST00000706955.1:c.*1104_*1106delinsAAT	ENSP00000516675.1:n.*1104_*1106delinsAAT
ENST00000686459.1:c.*655_*657delinsAAT	ENSP00000508909.1:n.*655_*657delinsAAT
ENST00000688158.1:c.*1180_*1182delinsAAT	ENSP00000509254.1:n.*1180_*1182delinsAAT
ENST00000688308.1:c.1069_1071delinsAAT	ENSP00000508752.1:p.Pro357Asn
ENST00000688922.1:c.990_992delinsAAT
ENST00000693560.1:c.1588_1590delinsAAT	ENSP00000509861.1:p.Pro530Asn
ENST00000371953.8:c.1069_1071delinsAAT MANE Select	ENSP00000361021.3:p.Pro357Asn
ENST00000371953.7:c.1069_1071delinsAAT	ENSP00000361021.3:p.Pro357Asn
NM_000314.5:c.1069_1071delinsAAT	NP_000305.3:p.Pro357Asn
NM_000314.6:c.1069_1071delinsAAT	NP_000305.3:p.Pro357Asn
NM_001304717.2:c.1588_1590delinsAAT	NP_001291646.2:p.Pro530Asn
NM_001304718.1:c.478_480delinsAAT	NP_001291647.1:p.Pro160Asn
XM_006717926.2:c.1024_1026delinsAAT	XP_006717989.1:p.Pro342Asn
XM_011539982.1:c.973_975delinsAAT	XP_011538284.1:p.Pro325Asn
XR_945791.1:n.1639_1641delinsAAT
NM_000314.7:c.1069_1071delinsAAT	NP_000305.3:p.Pro357Asn
NM_001304717.5:c.1588_1590delinsAAT	NP_001291646.4:p.Pro530Asn
NM_001304718.2:c.478_480delinsAAT	NP_001291647.1:p.Pro160Asn
NM_000314.8:c.1069_1071delinsAAT MANE Select	NP_000305.3:p.Pro357Asn