Canonical Allele Identifier: CA470669361

Gene: PTEN

Linked Data

• dbSNP Id: rs2132276646
• MyVariant Identifiers: chr10:g.89717644G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957887G>A , CM000672.2:g.87957887G>A	GRCh38
NC_000010.10:g.89717644G>A , CM000672.1:g.89717644G>A	GRCh37
NC_000010.9:g.89707624G>A	NCBI36
NG_007466.2:g.99449G>A , LRG_311:g.99449G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.669G>A	ENSP00000514759.2:p.Lys223=
ENST00000710265.1:c.669G>A	ENSP00000518161.1:p.Lys223=
ENST00000472832.3:c.669G>A	ENSP00000483066.2:p.Lys223=
ENST00000688158.2:n.1404G>A
ENST00000688922.2:c.*499G>A	ENSP00000508742.2:n.*499G>A
ENST00000700021.1:c.624G>A	ENSP00000514757.1:p.Lys208=
ENST00000700022.1:c.*8G>A	ENSP00000514758.1:n.*8G>A
ENST00000700023.1:n.1827G>A
ENST00000700024.1:n.2061G>A
ENST00000700025.1:n.1438G>A
ENST00000700026.1:n.306G>A
ENST00000700029.1:c.503G>A
ENST00000706954.1:c.669G>A	ENSP00000516674.1:p.Lys223=
ENST00000706955.1:c.*704G>A	ENSP00000516675.1:n.*704G>A
ENST00000686459.1:c.*255G>A	ENSP00000508909.1:n.*255G>A
ENST00000688158.1:c.*780G>A	ENSP00000509254.1:n.*780G>A
ENST00000688308.1:c.669G>A	ENSP00000508752.1:p.Lys223=
ENST00000688922.1:c.590G>A
ENST00000693560.1:c.1188G>A	ENSP00000509861.1:p.Lys396=
ENST00000371953.8:c.669G>A MANE Select	ENSP00000361021.3:p.Lys223=
ENST00000371953.7:c.669G>A	ENSP00000361021.3:p.Lys223=
ENST00000472832.2:c.96G>A	ENSP00000483066.1:p.Lys32=
NM_000314.5:c.669G>A	NP_000305.3:p.Lys223=
NM_000314.6:c.669G>A	NP_000305.3:p.Lys223=
NM_001304717.2:c.1188G>A	NP_001291646.2:p.Lys396=
NM_001304718.1:c.78G>A	NP_001291647.1:p.Lys26=
XM_006717926.2:c.624G>A	XP_006717989.1:p.Lys208=
XM_011539981.1:c.669G>A	XP_011538283.1:p.Lys223=
XM_011539982.1:c.573G>A	XP_011538284.1:p.Lys191=
XR_945791.1:n.1239G>A
NM_000314.7:c.669G>A	NP_000305.3:p.Lys223=
NM_001304717.5:c.1188G>A	NP_001291646.4:p.Lys396=
NM_001304718.2:c.78G>A	NP_001291647.1:p.Lys26=
NM_000314.8:c.669G>A MANE Select	NP_000305.3:p.Lys223=