Canonical Allele Identifier: CA470973949

Gene: PTEN

Linked Data

• dbSNP Id: rs876660443
• MyVariant Identifiers: chr10:g.89720707C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960950C>A , CM000672.2:g.87960950C>A	GRCh38
NC_000010.10:g.89720707C>A , CM000672.1:g.89720707C>A	GRCh37
NC_000010.9:g.89710687C>A	NCBI36
NG_007466.2:g.102512C>A , LRG_311:g.102512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.951C>A	ENSP00000514759.2:p.Thr317=
ENST00000710265.1:c.858C>A	ENSP00000518161.1:p.Thr286=
ENST00000472832.3:c.858C>A	ENSP00000483066.2:p.Thr286=
ENST00000688158.2:n.1593C>A
ENST00000688922.2:c.*688C>A	ENSP00000508742.2:n.*688C>A
ENST00000700021.1:c.813C>A	ENSP00000514757.1:p.Thr271=
ENST00000700022.1:c.*197C>A	ENSP00000514758.1:n.*197C>A
ENST00000700023.1:n.2016C>A
ENST00000700024.1:n.2250C>A
ENST00000700025.1:n.1627C>A
ENST00000700026.1:n.495C>A
ENST00000700029.1:c.785C>A
ENST00000706954.1:c.858C>A	ENSP00000516674.1:p.Thr286=
ENST00000706955.1:c.*893C>A	ENSP00000516675.1:n.*893C>A
ENST00000686459.1:c.*444C>A	ENSP00000508909.1:n.*444C>A
ENST00000688158.1:c.*969C>A	ENSP00000509254.1:n.*969C>A
ENST00000688308.1:c.858C>A	ENSP00000508752.1:p.Thr286=
ENST00000688922.1:c.779C>A
ENST00000693560.1:c.1377C>A	ENSP00000509861.1:p.Thr459=
ENST00000371953.8:c.858C>A MANE Select	ENSP00000361021.3:p.Thr286=
ENST00000371953.7:c.858C>A	ENSP00000361021.3:p.Thr286=
ENST00000472832.2:c.285C>A	ENSP00000483066.1:p.Thr95=
NM_000314.5:c.858C>A	NP_000305.3:p.Thr286=
NM_000314.6:c.858C>A	NP_000305.3:p.Thr286=
NM_001304717.2:c.1377C>A	NP_001291646.2:p.Thr459=
NM_001304718.1:c.267C>A	NP_001291647.1:p.Thr89=
XM_006717926.2:c.813C>A	XP_006717989.1:p.Thr271=
XM_011539981.1:c.858C>A	XP_011538283.1:p.Thr286=
XM_011539982.1:c.762C>A	XP_011538284.1:p.Thr254=
XR_945791.1:n.1428C>A
NM_000314.7:c.858C>A	NP_000305.3:p.Thr286=
NM_001304717.5:c.1377C>A	NP_001291646.4:p.Thr459=
NM_001304718.2:c.267C>A	NP_001291647.1:p.Thr89=
NM_000314.8:c.858C>A MANE Select	NP_000305.3:p.Thr286=