Canonical Allele Identifier: CA1926173932

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965376T= , CM000672.2:g.87965376T=	GRCh38
NC_000010.10:g.89725133T= , CM000672.1:g.89725133T=	GRCh37
NC_000010.9:g.89715113T=	NCBI36
NG_007466.2:g.106938T= , LRG_311:g.106938T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1209T=	ENSP00000514759.2:p.Asn403=
ENST00000710265.1:c.*145T=	ENSP00000518161.1:n.*145T=
ENST00000688158.2:n.1851T=
ENST00000688922.2:c.*946T=	ENSP00000508742.2:n.*946T=
ENST00000700021.1:c.1071T=	ENSP00000514757.1:p.Asn357=
ENST00000700022.1:c.*455T=	ENSP00000514758.1:n.*455T=
ENST00000700023.1:n.2274T=
ENST00000700024.1:n.2508T=
ENST00000706954.1:c.1116T=	ENSP00000516674.1:p.Asn372=
ENST00000706955.1:c.*1151T=	ENSP00000516675.1:n.*1151T=
ENST00000686459.1:c.*702T=	ENSP00000508909.1:n.*702T=
ENST00000688158.1:c.*1227T=	ENSP00000509254.1:n.*1227T=
ENST00000688308.1:c.1116T=	ENSP00000508752.1:p.Asn372=
ENST00000688922.1:c.1037T=
ENST00000693560.1:c.1635T=	ENSP00000509861.1:p.Asn545=
ENST00000371953.8:c.1116T= MANE Select	ENSP00000361021.3:p.Asn372=
ENST00000371953.7:c.1116T=	ENSP00000361021.3:p.Asn372=
NM_000314.5:c.1116T=	NP_000305.3:p.Asn372=
NM_000314.6:c.1116T=	NP_000305.3:p.Asn372=
NM_001304717.2:c.1635T=	NP_001291646.2:p.Asn545=
NM_001304718.1:c.525T=	NP_001291647.1:p.Asn175=
XM_006717926.2:c.1071T=	XP_006717989.1:p.Asn357=
XM_011539982.1:c.1020T=	XP_011538284.1:p.Asn340=
XR_945791.1:n.1686T=
NM_000314.7:c.1116T=	NP_000305.3:p.Asn372=
NM_001304717.5:c.1635T=	NP_001291646.4:p.Asn545=
NM_001304718.2:c.525T=	NP_001291647.1:p.Asn175=
NM_000314.8:c.1116T= MANE Select	NP_000305.3:p.Asn372=