Canonical Allele Identifier: CA378713188

Gene: MGMT

Linked Data

• dbSNP Id: rs1848944428
• gnomAD v4: 10-129766918-G-A
• COSMIC: COSM384220
• MyVariant Identifiers: chr10:g.131565182G>A (hg19) ; chr10:g.129766918G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766918G>A , CM000672.2:g.129766918G>A	GRCh38
NC_000010.10:g.131565182G>A , CM000672.1:g.131565182G>A	GRCh37
NC_000010.9:g.131455172G>A	NCBI36
NG_052673.1:g.304735G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.638G>A	ENSP00000302111.7:p.Gly213Glu
ENST00000651593.1:c.545G>A MANE Select	ENSP00000498729.1:p.Gly182Glu
ENST00000306010.7:c.638G>A	ENSP00000302111.7:p.Gly213Glu
NM_002412.3:c.638G>A	NP_002403.2:p.Gly213Glu
NM_002412.4:c.638G>A	NP_002403.2:p.Gly213Glu
XM_005252682.2:c.545G>A	XP_005252739.1:p.Gly182Glu
XM_006717863.2:c.368G>A	XP_006717926.1:p.Gly123Glu
XM_011539817.1:c.554G>A	XP_011538119.1:p.Gly185Glu
NM_002412.5:c.545G>A MANE Select	NP_002403.3:p.Gly182Glu
XM_017016275.1:c.368G>A	XP_016871764.1:p.Gly123Glu