Canonical Allele Identifier: CA891837250

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965330_87965331delinsAT , CM000672.2:g.87965330_87965331delinsAT	GRCh38
NC_000010.10:g.89725087_89725088delinsAT , CM000672.1:g.89725087_89725088delinsAT	GRCh37
NC_000010.9:g.89715067_89715068delinsAT	NCBI36
NG_007466.2:g.106892_106893delinsAT , LRG_311:g.106892_106893delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1163_1164delinsAT	ENSP00000514759.2:p.Pro388His
ENST00000710265.1:c.*99_*100delinsAT	ENSP00000518161.1:n.*99_*100delinsAT
ENST00000688158.2:n.1805_1806delinsAT
ENST00000688922.2:c.*900_*901delinsAT	ENSP00000508742.2:n.*900_*901delinsAT
ENST00000700021.1:c.1025_1026delinsAT	ENSP00000514757.1:p.Pro342His
ENST00000700022.1:c.*409_*410delinsAT	ENSP00000514758.1:n.*409_*410delinsAT
ENST00000700023.1:n.2228_2229delinsAT
ENST00000700024.1:n.2462_2463delinsAT
ENST00000706954.1:c.1070_1071delinsAT	ENSP00000516674.1:p.Pro357His
ENST00000706955.1:c.*1105_*1106delinsAT	ENSP00000516675.1:n.*1105_*1106delinsAT
ENST00000686459.1:c.*656_*657delinsAT	ENSP00000508909.1:n.*656_*657delinsAT
ENST00000688158.1:c.*1181_*1182delinsAT	ENSP00000509254.1:n.*1181_*1182delinsAT
ENST00000688308.1:c.1070_1071delinsAT	ENSP00000508752.1:p.Pro357His
ENST00000688922.1:c.991_992delinsAT
ENST00000693560.1:c.1589_1590delinsAT	ENSP00000509861.1:p.Pro530His
ENST00000371953.8:c.1070_1071delinsAT MANE Select	ENSP00000361021.3:p.Pro357His
ENST00000371953.7:c.1070_1071delinsAT	ENSP00000361021.3:p.Pro357His
NM_000314.5:c.1070_1071delinsAT	NP_000305.3:p.Pro357His
NM_000314.6:c.1070_1071delinsAT	NP_000305.3:p.Pro357His
NM_001304717.2:c.1589_1590delinsAT	NP_001291646.2:p.Pro530His
NM_001304718.1:c.479_480delinsAT	NP_001291647.1:p.Pro160His
XM_006717926.2:c.1025_1026delinsAT	XP_006717989.1:p.Pro342His
XM_011539982.1:c.974_975delinsAT	XP_011538284.1:p.Pro325His
XR_945791.1:n.1640_1641delinsAT
NM_000314.7:c.1070_1071delinsAT	NP_000305.3:p.Pro357His
NM_001304717.5:c.1589_1590delinsAT	NP_001291646.4:p.Pro530His
NM_001304718.2:c.479_480delinsAT	NP_001291647.1:p.Pro160His
NM_000314.8:c.1070_1071delinsAT MANE Select	NP_000305.3:p.Pro357His