Canonical Allele Identifier: CA1926173962

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965388T= , CM000672.2:g.87965388T=	GRCh38
NC_000010.10:g.89725145T= , CM000672.1:g.89725145T=	GRCh37
NC_000010.9:g.89715125T=	NCBI36
NG_007466.2:g.106950T= , LRG_311:g.106950T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1221T=	ENSP00000514759.2:p.His407=
ENST00000710265.1:c.*157T=	ENSP00000518161.1:n.*157T=
ENST00000688158.2:n.1863T=
ENST00000688922.2:c.*958T=	ENSP00000508742.2:n.*958T=
ENST00000700021.1:c.1083T=	ENSP00000514757.1:p.His361=
ENST00000700022.1:c.*467T=	ENSP00000514758.1:n.*467T=
ENST00000700023.1:n.2286T=
ENST00000700024.1:n.2520T=
ENST00000706954.1:c.1128T=	ENSP00000516674.1:p.His376=
ENST00000706955.1:c.*1163T=	ENSP00000516675.1:n.*1163T=
ENST00000686459.1:c.*714T=	ENSP00000508909.1:n.*714T=
ENST00000688158.1:c.*1239T=	ENSP00000509254.1:n.*1239T=
ENST00000688308.1:c.1128T=	ENSP00000508752.1:p.His376=
ENST00000688922.1:c.1049T=
ENST00000693560.1:c.1647T=	ENSP00000509861.1:p.His549=
ENST00000371953.8:c.1128T= MANE Select	ENSP00000361021.3:p.His376=
ENST00000371953.7:c.1128T=	ENSP00000361021.3:p.His376=
NM_000314.5:c.1128T=	NP_000305.3:p.His376=
NM_000314.6:c.1128T=	NP_000305.3:p.His376=
NM_001304717.2:c.1647T=	NP_001291646.2:p.His549=
NM_001304718.1:c.537T=	NP_001291647.1:p.His179=
XM_006717926.2:c.1083T=	XP_006717989.1:p.His361=
XM_011539982.1:c.1032T=	XP_011538284.1:p.His344=
XR_945791.1:n.1698T=
NM_000314.7:c.1128T=	NP_000305.3:p.His376=
NM_001304717.5:c.1647T=	NP_001291646.4:p.His549=
NM_001304718.2:c.537T=	NP_001291647.1:p.His179=
NM_000314.8:c.1128T= MANE Select	NP_000305.3:p.His376=