Canonical Allele Identifier: CA470669124

Gene: PTEN

Linked Data

• dbSNP Id: rs2132276405
• MyVariant Identifiers: chr10:g.89717614T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957857T>A , CM000672.2:g.87957857T>A	GRCh38
NC_000010.10:g.89717614T>A , CM000672.1:g.89717614T>A	GRCh37
NC_000010.9:g.89707594T>A	NCBI36
NG_007466.2:g.99419T>A , LRG_311:g.99419T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.639T>A	ENSP00000514759.2:p.Pro213=
ENST00000710265.1:c.639T>A	ENSP00000518161.1:p.Pro213=
ENST00000472832.3:c.639T>A	ENSP00000483066.2:p.Pro213=
ENST00000688158.2:n.1374T>A
ENST00000688922.2:c.*469T>A	ENSP00000508742.2:n.*469T>A
ENST00000700021.1:c.594T>A	ENSP00000514757.1:p.Pro198=
ENST00000700022.1:c.497T>A	ENSP00000514758.1:p.Leu166His
ENST00000700023.1:n.1797T>A
ENST00000700024.1:n.2031T>A
ENST00000700025.1:n.1408T>A
ENST00000700026.1:n.276T>A
ENST00000700029.1:c.473T>A
ENST00000706954.1:c.639T>A	ENSP00000516674.1:p.Pro213=
ENST00000706955.1:c.*674T>A	ENSP00000516675.1:n.*674T>A
ENST00000686459.1:c.*225T>A	ENSP00000508909.1:n.*225T>A
ENST00000688158.1:c.*750T>A	ENSP00000509254.1:n.*750T>A
ENST00000688308.1:c.639T>A	ENSP00000508752.1:p.Pro213=
ENST00000688922.1:c.560T>A
ENST00000693560.1:c.1158T>A	ENSP00000509861.1:p.Pro386=
ENST00000371953.8:c.639T>A MANE Select	ENSP00000361021.3:p.Pro213=
ENST00000371953.7:c.639T>A	ENSP00000361021.3:p.Pro213=
ENST00000472832.2:c.66T>A	ENSP00000483066.1:p.Pro22=
NM_000314.5:c.639T>A	NP_000305.3:p.Pro213=
NM_000314.6:c.639T>A	NP_000305.3:p.Pro213=
NM_001304717.2:c.1158T>A	NP_001291646.2:p.Pro386=
NM_001304718.1:c.48T>A	NP_001291647.1:p.Pro16=
XM_006717926.2:c.594T>A	XP_006717989.1:p.Pro198=
XM_011539981.1:c.639T>A	XP_011538283.1:p.Pro213=
XM_011539982.1:c.543T>A	XP_011538284.1:p.Pro181=
XR_945791.1:n.1209T>A
NM_000314.7:c.639T>A	NP_000305.3:p.Pro213=
NM_001304717.5:c.1158T>A	NP_001291646.4:p.Pro386=
NM_001304718.2:c.48T>A	NP_001291647.1:p.Pro16=
NM_000314.8:c.639T>A MANE Select	NP_000305.3:p.Pro213=