Canonical Allele Identifier: CA1926190065

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961037T= , CM000672.2:g.87961037T=	GRCh38
NC_000010.10:g.89720794T= , CM000672.1:g.89720794T=	GRCh37
NC_000010.9:g.89710774T=	NCBI36
NG_007466.2:g.102599T= , LRG_311:g.102599T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1038T=	ENSP00000514759.2:p.Tyr346=
ENST00000710265.1:c.945T=	ENSP00000518161.1:p.Tyr315=
ENST00000472832.3:c.945T=	ENSP00000483066.2:p.Tyr315=
ENST00000688158.2:n.1680T=
ENST00000688922.2:c.*775T=	ENSP00000508742.2:n.*775T=
ENST00000700021.1:c.900T=	ENSP00000514757.1:p.Tyr300=
ENST00000700022.1:c.*284T=	ENSP00000514758.1:n.*284T=
ENST00000700023.1:n.2103T=
ENST00000700024.1:n.2337T=
ENST00000700025.1:n.1714T=
ENST00000700026.1:n.582T=
ENST00000706954.1:c.945T=	ENSP00000516674.1:p.Tyr315=
ENST00000706955.1:c.*980T=	ENSP00000516675.1:n.*980T=
ENST00000686459.1:c.*531T=	ENSP00000508909.1:n.*531T=
ENST00000688158.1:c.*1056T=	ENSP00000509254.1:n.*1056T=
ENST00000688308.1:c.945T=	ENSP00000508752.1:p.Tyr315=
ENST00000688922.1:c.866T=
ENST00000693560.1:c.1464T=	ENSP00000509861.1:p.Tyr488=
ENST00000371953.8:c.945T= MANE Select	ENSP00000361021.3:p.Tyr315=
ENST00000371953.7:c.945T=	ENSP00000361021.3:p.Tyr315=
ENST00000472832.2:c.372T=	ENSP00000483066.1:p.Tyr124=
NM_000314.5:c.945T=	NP_000305.3:p.Tyr315=
NM_000314.6:c.945T=	NP_000305.3:p.Tyr315=
NM_001304717.2:c.1464T=	NP_001291646.2:p.Tyr488=
NM_001304718.1:c.354T=	NP_001291647.1:p.Tyr118=
XM_006717926.2:c.900T=	XP_006717989.1:p.Tyr300=
XM_011539981.1:c.945T=	XP_011538283.1:p.Tyr315=
XM_011539982.1:c.849T=	XP_011538284.1:p.Tyr283=
XR_945791.1:n.1515T=
NM_000314.7:c.945T=	NP_000305.3:p.Tyr315=
NM_001304717.5:c.1464T=	NP_001291646.4:p.Tyr488=
NM_001304718.2:c.354T=	NP_001291647.1:p.Tyr118=
NM_000314.8:c.945T= MANE Select	NP_000305.3:p.Tyr315=