Canonical Allele Identifier: CA1926175629

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966841T= , CM000672.2:g.87966841T=	GRCh38
NC_000010.10:g.89726598T= , CM000672.1:g.89726598T=	GRCh37
NC_000010.9:g.89716578T=	NCBI36
NG_007466.2:g.108403T= , LRG_311:g.108403T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1369T=	ENSP00000514759.2:n.*1369T=
ENST00000710265.1:c.*1610T=	ENSP00000518161.1:n.*1610T=
ENST00000688158.2:n.3316T=
ENST00000688922.2:c.*2411T=	ENSP00000508742.2:n.*2411T=
ENST00000700021.1:c.*1369T=	ENSP00000514757.1:n.*1369T=
ENST00000700024.1:n.3973T=
ENST00000706954.1:c.*1369T=	ENSP00000516674.1:n.*1369T=
ENST00000706955.1:c.*2616T=	ENSP00000516675.1:n.*2616T=
ENST00000688158.1:c.*2692T=	ENSP00000509254.1:n.*2692T=
ENST00000688308.1:c.*1369T=	ENSP00000508752.1:n.*1369T=
ENST00000688922.1:c.2502T=
ENST00000693560.1:c.*1369T=	ENSP00000509861.1:n.*1369T=
ENST00000371953.8:c.*1369T= MANE Select	ENSP00000361021.3:n.*1369T=
ENST00000371953.7:c.*1369T=	ENSP00000361021.3:n.*1369T=
NM_000314.5:c.*1369T=	NP_000305.3:n.*1369T=
NM_000314.6:c.*1369T=	NP_000305.3:n.*1369T=
NM_001304717.2:c.*1369T=	NP_001291646.2:n.*1369T=
NM_001304718.1:c.*1369T=	NP_001291647.1:n.*1369T=
XM_006717926.2:c.*1369T=	XP_006717989.1:n.*1369T=
XM_011539982.1:c.*1369T=	XP_011538284.1:n.*1369T=
XR_945791.1:n.3151T=
NM_000314.7:c.*1369T=	NP_000305.3:n.*1369T=
NM_001304717.5:c.*1369T=	NP_001291646.4:n.*1369T=
NM_001304718.2:c.*1369T=	NP_001291647.1:n.*1369T=
NM_000314.8:c.*1369T= MANE Select	NP_000305.3:n.*1369T=