Canonical Allele Identifier: CA470669203

Gene: PTEN

Linked Data

• dbSNP Id: rs886038278
• MyVariant Identifiers: chr10:g.89717626C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957869C>G , CM000672.2:g.87957869C>G	GRCh38
NC_000010.10:g.89717626C>G , CM000672.1:g.89717626C>G	GRCh37
NC_000010.9:g.89707606C>G	NCBI36
NG_007466.2:g.99431C>G , LRG_311:g.99431C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.651C>G	ENSP00000514759.2:p.Val217=
ENST00000710265.1:c.651C>G	ENSP00000518161.1:p.Val217=
ENST00000472832.3:c.651C>G	ENSP00000483066.2:p.Val217=
ENST00000688158.2:n.1386C>G
ENST00000688922.2:c.*481C>G	ENSP00000508742.2:n.*481C>G
ENST00000700021.1:c.606C>G	ENSP00000514757.1:p.Val202=
ENST00000700022.1:c.509C>G	ENSP00000514758.1:p.Ser170Cys
ENST00000700023.1:n.1809C>G
ENST00000700024.1:n.2043C>G
ENST00000700025.1:n.1420C>G
ENST00000700026.1:n.288C>G
ENST00000700029.1:c.485C>G
ENST00000706954.1:c.651C>G	ENSP00000516674.1:p.Val217=
ENST00000706955.1:c.*686C>G	ENSP00000516675.1:n.*686C>G
ENST00000686459.1:c.*237C>G	ENSP00000508909.1:n.*237C>G
ENST00000688158.1:c.*762C>G	ENSP00000509254.1:n.*762C>G
ENST00000688308.1:c.651C>G	ENSP00000508752.1:p.Val217=
ENST00000688922.1:c.572C>G
ENST00000693560.1:c.1170C>G	ENSP00000509861.1:p.Val390=
ENST00000371953.8:c.651C>G MANE Select	ENSP00000361021.3:p.Val217=
ENST00000371953.7:c.651C>G	ENSP00000361021.3:p.Val217=
ENST00000472832.2:c.78C>G	ENSP00000483066.1:p.Val26=
NM_000314.5:c.651C>G	NP_000305.3:p.Val217=
NM_000314.6:c.651C>G	NP_000305.3:p.Val217=
NM_001304717.2:c.1170C>G	NP_001291646.2:p.Val390=
NM_001304718.1:c.60C>G	NP_001291647.1:p.Val20=
XM_006717926.2:c.606C>G	XP_006717989.1:p.Val202=
XM_011539981.1:c.651C>G	XP_011538283.1:p.Val217=
XM_011539982.1:c.555C>G	XP_011538284.1:p.Val185=
XR_945791.1:n.1221C>G
NM_000314.7:c.651C>G	NP_000305.3:p.Val217=
NM_001304717.5:c.1170C>G	NP_001291646.4:p.Val390=
NM_001304718.2:c.60C>G	NP_001291647.1:p.Val20=
NM_000314.8:c.651C>G MANE Select	NP_000305.3:p.Val217=