Canonical Allele Identifier: CA1926174029

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965432C= , CM000672.2:g.87965432C=	GRCh38
NC_000010.10:g.89725189C= , CM000672.1:g.89725189C=	GRCh37
NC_000010.9:g.89715169C=	NCBI36
NG_007466.2:g.106994C= , LRG_311:g.106994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1265C=	ENSP00000514759.2:p.Pro422=
ENST00000710265.1:c.*201C=	ENSP00000518161.1:n.*201C=
ENST00000688158.2:n.1907C=
ENST00000688922.2:c.*1002C=	ENSP00000508742.2:n.*1002C=
ENST00000700021.1:c.1127C=	ENSP00000514757.1:p.Pro376=
ENST00000700022.1:c.*511C=	ENSP00000514758.1:n.*511C=
ENST00000700023.1:n.2330C=
ENST00000700024.1:n.2564C=
ENST00000706954.1:c.1172C=	ENSP00000516674.1:p.Pro391=
ENST00000706955.1:c.*1207C=	ENSP00000516675.1:n.*1207C=
ENST00000686459.1:c.*758C=	ENSP00000508909.1:n.*758C=
ENST00000688158.1:c.*1283C=	ENSP00000509254.1:n.*1283C=
ENST00000688308.1:c.1172C=	ENSP00000508752.1:p.Pro391=
ENST00000688922.1:c.1093C=
ENST00000693560.1:c.1691C=	ENSP00000509861.1:p.Pro564=
ENST00000371953.8:c.1172C= MANE Select	ENSP00000361021.3:p.Pro391=
ENST00000371953.7:c.1172C=	ENSP00000361021.3:p.Pro391=
NM_000314.5:c.1172C=	NP_000305.3:p.Pro391=
NM_000314.6:c.1172C=	NP_000305.3:p.Pro391=
NM_001304717.2:c.1691C=	NP_001291646.2:p.Pro564=
NM_001304718.1:c.581C=	NP_001291647.1:p.Pro194=
XM_006717926.2:c.1127C=	XP_006717989.1:p.Pro376=
XM_011539982.1:c.1076C=	XP_011538284.1:p.Pro359=
XR_945791.1:n.1742C=
NM_000314.7:c.1172C=	NP_000305.3:p.Pro391=
NM_001304717.5:c.1691C=	NP_001291646.4:p.Pro564=
NM_001304718.2:c.581C=	NP_001291647.1:p.Pro194=
NM_000314.8:c.1172C= MANE Select	NP_000305.3:p.Pro391=