Canonical Allele Identifier: CA5748158

Gene: MGMT

Linked Data

• dbSNP Id: rs781760384
• ExAC: 10:131565203 G / A
• gnomAD v2: 10-131565203-G-A
• gnomAD v3: 10-129766939-G-A
• gnomAD v4: 10-129766939-G-A
• MyVariant Identifiers: chr10:g.131565203G>A (hg19) ; chr10:g.129766939G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766939G>A , CM000672.2:g.129766939G>A	GRCh38
NC_000010.10:g.131565203G>A , CM000672.1:g.131565203G>A	GRCh37
NC_000010.9:g.131455193G>A	NCBI36
NG_052673.1:g.304756G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.659G>A	ENSP00000302111.7:p.Gly220Glu
ENST00000651593.1:c.566G>A MANE Select	ENSP00000498729.1:p.Gly189Glu
ENST00000306010.7:c.659G>A	ENSP00000302111.7:p.Gly220Glu
NM_002412.3:c.659G>A	NP_002403.2:p.Gly220Glu
NM_002412.4:c.659G>A	NP_002403.2:p.Gly220Glu
XM_005252682.2:c.566G>A	XP_005252739.1:p.Gly189Glu
XM_006717863.2:c.389G>A	XP_006717926.1:p.Gly130Glu
XM_011539817.1:c.575G>A	XP_011538119.1:p.Gly192Glu
NM_002412.5:c.566G>A MANE Select	NP_002403.3:p.Gly189Glu
XM_017016275.1:c.389G>A	XP_016871764.1:p.Gly130Glu