Canonical Allele Identifier: CA377482301

Gene: PTEN

Linked Data

• ClinVar Variation Id: 1508589
• ClinVar RCV Id: RCV002016214
• dbSNP Id: rs1114167656
• COSMIC: COSM4391544
• MyVariant Identifiers: chr10:g.89692893C>G (hg19) ; chr10:g.87933136C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933136C>G , CM000672.2:g.87933136C>G	GRCh38
NC_000010.10:g.89692893C>G , CM000672.1:g.89692893C>G	GRCh37
NC_000010.9:g.89682873C>G	NCBI36
NG_007466.2:g.74698C>G , LRG_311:g.74698C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.377C>G	ENSP00000514759.2:p.Ala126Gly
ENST00000710265.1:c.377C>G	ENSP00000518161.1:p.Ala126Gly
ENST00000472832.3:c.377C>G	ENSP00000483066.2:p.Ala126Gly
ENST00000688158.2:n.1112C>G
ENST00000688922.2:c.*207C>G	ENSP00000508742.2:n.*207C>G
ENST00000700021.1:c.332C>G	ENSP00000514757.1:p.Ala111Gly
ENST00000700022.1:c.377C>G	ENSP00000514758.1:p.Ala126Gly
ENST00000700029.1:c.211C>G
ENST00000706954.1:c.377C>G	ENSP00000516674.1:p.Ala126Gly
ENST00000706955.1:c.*412C>G	ENSP00000516675.1:n.*412C>G
ENST00000686459.1:c.377C>G	ENSP00000508909.1:p.Ala126Gly
ENST00000688158.1:c.*488C>G	ENSP00000509254.1:n.*488C>G
ENST00000688308.1:c.377C>G	ENSP00000508752.1:p.Ala126Gly
ENST00000688922.1:c.298C>G
ENST00000693560.1:c.896C>G	ENSP00000509861.1:p.Ala299Gly
ENST00000371953.8:c.377C>G MANE Select	ENSP00000361021.3:p.Ala126Gly
ENST00000371953.7:c.377C>G	ENSP00000361021.3:p.Ala126Gly
ENST00000498703.1:n.203C>G
ENST00000610634.1:c.275C>G	ENSP00000477517.1:p.Ala92Gly
NM_000314.5:c.377C>G	NP_000305.3:p.Ala126Gly
NM_000314.6:c.377C>G	NP_000305.3:p.Ala126Gly
NM_001304717.2:c.896C>G	NP_001291646.2:p.Ala299Gly
NM_001304718.1:c.-374C>G	NP_001291647.1:n.-374C>G
XM_006717926.2:c.332C>G	XP_006717989.1:p.Ala111Gly
XM_011539981.1:c.377C>G	XP_011538283.1:p.Ala126Gly
XM_011539982.1:c.281C>G	XP_011538284.1:p.Ala94Gly
XR_945789.1:n.1089C>G
XR_945790.1:n.1089C>G
XR_945791.1:n.1089C>G
NM_000314.7:c.377C>G	NP_000305.3:p.Ala126Gly
NM_001304717.5:c.896C>G	NP_001291646.4:p.Ala299Gly
NM_001304718.2:c.-374C>G	NP_001291647.1:n.-374C>G
NM_000314.8:c.377C>G MANE Select	NP_000305.3:p.Ala126Gly