Canonical Allele Identifier: CA1926174192

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965501C= , CM000672.2:g.87965501C=	GRCh38
NC_000010.10:g.89725258C= , CM000672.1:g.89725258C=	GRCh37
NC_000010.9:g.89715238C=	NCBI36
NG_007466.2:g.107063C= , LRG_311:g.107063C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*29C=	ENSP00000514759.2:n.*29C=
ENST00000710265.1:c.*270C=	ENSP00000518161.1:n.*270C=
ENST00000688158.2:n.1976C=
ENST00000688922.2:c.*1071C=	ENSP00000508742.2:n.*1071C=
ENST00000700021.1:c.*29C=	ENSP00000514757.1:n.*29C=
ENST00000700022.1:c.*580C=	ENSP00000514758.1:n.*580C=
ENST00000700023.1:n.2399C=
ENST00000700024.1:n.2633C=
ENST00000706954.1:c.*29C=	ENSP00000516674.1:n.*29C=
ENST00000706955.1:c.*1276C=	ENSP00000516675.1:n.*1276C=
ENST00000686459.1:c.*827C=	ENSP00000508909.1:n.*827C=
ENST00000688158.1:c.*1352C=	ENSP00000509254.1:n.*1352C=
ENST00000688308.1:c.*29C=	ENSP00000508752.1:n.*29C=
ENST00000688922.1:c.1162C=
ENST00000693560.1:c.*29C=	ENSP00000509861.1:n.*29C=
ENST00000371953.8:c.*29C= MANE Select	ENSP00000361021.3:n.*29C=
ENST00000371953.7:c.*29C=	ENSP00000361021.3:n.*29C=
NM_000314.5:c.*29C=	NP_000305.3:n.*29C=
NM_000314.6:c.*29C=	NP_000305.3:n.*29C=
NM_001304717.2:c.*29C=	NP_001291646.2:n.*29C=
NM_001304718.1:c.*29C=	NP_001291647.1:n.*29C=
XM_006717926.2:c.*29C=	XP_006717989.1:n.*29C=
XM_011539982.1:c.*29C=	XP_011538284.1:n.*29C=
XR_945791.1:n.1811C=
NM_000314.7:c.*29C=	NP_000305.3:n.*29C=
NM_001304717.5:c.*29C=	NP_001291646.4:n.*29C=
NM_001304718.2:c.*29C=	NP_001291647.1:n.*29C=
NM_000314.8:c.*29C= MANE Select	NP_000305.3:n.*29C=