Canonical Allele Identifier: CA1926175597

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966827C= , CM000672.2:g.87966827C=	GRCh38
NC_000010.10:g.89726584C= , CM000672.1:g.89726584C=	GRCh37
NC_000010.9:g.89716564C=	NCBI36
NG_007466.2:g.108389C= , LRG_311:g.108389C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1355C=	ENSP00000514759.2:n.*1355C=
ENST00000710265.1:c.*1596C=	ENSP00000518161.1:n.*1596C=
ENST00000688158.2:n.3302C=
ENST00000688922.2:c.*2397C=	ENSP00000508742.2:n.*2397C=
ENST00000700021.1:c.*1355C=	ENSP00000514757.1:n.*1355C=
ENST00000700024.1:n.3959C=
ENST00000706954.1:c.*1355C=	ENSP00000516674.1:n.*1355C=
ENST00000706955.1:c.*2602C=	ENSP00000516675.1:n.*2602C=
ENST00000688158.1:c.*2678C=	ENSP00000509254.1:n.*2678C=
ENST00000688308.1:c.*1355C=	ENSP00000508752.1:n.*1355C=
ENST00000688922.1:c.2488C=
ENST00000693560.1:c.*1355C=	ENSP00000509861.1:n.*1355C=
ENST00000371953.8:c.*1355C= MANE Select	ENSP00000361021.3:n.*1355C=
ENST00000371953.7:c.*1355C=	ENSP00000361021.3:n.*1355C=
NM_000314.5:c.*1355C=	NP_000305.3:n.*1355C=
NM_000314.6:c.*1355C=	NP_000305.3:n.*1355C=
NM_001304717.2:c.*1355C=	NP_001291646.2:n.*1355C=
NM_001304718.1:c.*1355C=	NP_001291647.1:n.*1355C=
XM_006717926.2:c.*1355C=	XP_006717989.1:n.*1355C=
XM_011539982.1:c.*1355C=	XP_011538284.1:n.*1355C=
XR_945791.1:n.3137C=
NM_000314.7:c.*1355C=	NP_000305.3:n.*1355C=
NM_001304717.5:c.*1355C=	NP_001291646.4:n.*1355C=
NM_001304718.2:c.*1355C=	NP_001291647.1:n.*1355C=
NM_000314.8:c.*1355C= MANE Select	NP_000305.3:n.*1355C=