Canonical Allele Identifier: CA470974049

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720806T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961049T>A , CM000672.2:g.87961049T>A	GRCh38
NC_000010.10:g.89720806T>A , CM000672.1:g.89720806T>A	GRCh37
NC_000010.9:g.89710786T>A	NCBI36
NG_007466.2:g.102611T>A , LRG_311:g.102611T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1050T>A	ENSP00000514759.2:p.Thr350=
ENST00000710265.1:c.957T>A	ENSP00000518161.1:p.Thr319=
ENST00000472832.3:c.957T>A	ENSP00000483066.2:p.Thr319=
ENST00000688158.2:n.1692T>A
ENST00000688922.2:c.*787T>A	ENSP00000508742.2:n.*787T>A
ENST00000700021.1:c.912T>A	ENSP00000514757.1:p.Thr304=
ENST00000700022.1:c.*296T>A	ENSP00000514758.1:n.*296T>A
ENST00000700023.1:n.2115T>A
ENST00000700024.1:n.2349T>A
ENST00000700025.1:n.1726T>A
ENST00000700026.1:n.594T>A
ENST00000706954.1:c.957T>A	ENSP00000516674.1:p.Thr319=
ENST00000706955.1:c.*992T>A	ENSP00000516675.1:n.*992T>A
ENST00000686459.1:c.*543T>A	ENSP00000508909.1:n.*543T>A
ENST00000688158.1:c.*1068T>A	ENSP00000509254.1:n.*1068T>A
ENST00000688308.1:c.957T>A	ENSP00000508752.1:p.Thr319=
ENST00000688922.1:c.878T>A
ENST00000693560.1:c.1476T>A	ENSP00000509861.1:p.Thr492=
ENST00000371953.8:c.957T>A MANE Select	ENSP00000361021.3:p.Thr319=
ENST00000371953.7:c.957T>A	ENSP00000361021.3:p.Thr319=
ENST00000472832.2:c.384T>A	ENSP00000483066.1:p.Thr128=
NM_000314.5:c.957T>A	NP_000305.3:p.Thr319=
NM_000314.6:c.957T>A	NP_000305.3:p.Thr319=
NM_001304717.2:c.1476T>A	NP_001291646.2:p.Thr492=
NM_001304718.1:c.366T>A	NP_001291647.1:p.Thr122=
XM_006717926.2:c.912T>A	XP_006717989.1:p.Thr304=
XM_011539981.1:c.957T>A	XP_011538283.1:p.Thr319=
XM_011539982.1:c.861T>A	XP_011538284.1:p.Thr287=
XR_945791.1:n.1527T>A
NM_000314.7:c.957T>A	NP_000305.3:p.Thr319=
NM_001304717.5:c.1476T>A	NP_001291646.4:p.Thr492=
NM_001304718.2:c.366T>A	NP_001291647.1:p.Thr122=
NM_000314.8:c.957T>A MANE Select	NP_000305.3:p.Thr319=