Canonical Allele Identifier: CA891841573

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965329_87965330delinsGT , CM000672.2:g.87965329_87965330delinsGT	GRCh38
NC_000010.10:g.89725086_89725087delinsGT , CM000672.1:g.89725086_89725087delinsGT	GRCh37
NC_000010.9:g.89715066_89715067delinsGT	NCBI36
NG_007466.2:g.106891_106892delinsGT , LRG_311:g.106891_106892delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1162_1163delinsGT	ENSP00000514759.2:p.Pro388Val
ENST00000710265.1:c.*98_*99delinsGT	ENSP00000518161.1:n.*98_*99delinsGT
ENST00000688158.2:n.1804_1805delinsGT
ENST00000688922.2:c.*899_*900delinsGT	ENSP00000508742.2:n.*899_*900delinsGT
ENST00000700021.1:c.1024_1025delinsGT	ENSP00000514757.1:p.Pro342Val
ENST00000700022.1:c.*408_*409delinsGT	ENSP00000514758.1:n.*408_*409delinsGT
ENST00000700023.1:n.2227_2228delinsGT
ENST00000700024.1:n.2461_2462delinsGT
ENST00000706954.1:c.1069_1070delinsGT	ENSP00000516674.1:p.Pro357Val
ENST00000706955.1:c.*1104_*1105delinsGT	ENSP00000516675.1:n.*1104_*1105delinsGT
ENST00000686459.1:c.*655_*656delinsGT	ENSP00000508909.1:n.*655_*656delinsGT
ENST00000688158.1:c.*1180_*1181delinsGT	ENSP00000509254.1:n.*1180_*1181delinsGT
ENST00000688308.1:c.1069_1070delinsGT	ENSP00000508752.1:p.Pro357Val
ENST00000688922.1:c.990_991delinsGT
ENST00000693560.1:c.1588_1589delinsGT	ENSP00000509861.1:p.Pro530Val
ENST00000371953.8:c.1069_1070delinsGT MANE Select	ENSP00000361021.3:p.Pro357Val
ENST00000371953.7:c.1069_1070delinsGT	ENSP00000361021.3:p.Pro357Val
NM_000314.5:c.1069_1070delinsGT	NP_000305.3:p.Pro357Val
NM_000314.6:c.1069_1070delinsGT	NP_000305.3:p.Pro357Val
NM_001304717.2:c.1588_1589delinsGT	NP_001291646.2:p.Pro530Val
NM_001304718.1:c.478_479delinsGT	NP_001291647.1:p.Pro160Val
XM_006717926.2:c.1024_1025delinsGT	XP_006717989.1:p.Pro342Val
XM_011539982.1:c.973_974delinsGT	XP_011538284.1:p.Pro325Val
XR_945791.1:n.1639_1640delinsGT
NM_000314.7:c.1069_1070delinsGT	NP_000305.3:p.Pro357Val
NM_001304717.5:c.1588_1589delinsGT	NP_001291646.4:p.Pro530Val
NM_001304718.2:c.478_479delinsGT	NP_001291647.1:p.Pro160Val
NM_000314.8:c.1069_1070delinsGT MANE Select	NP_000305.3:p.Pro357Val