Canonical Allele Identifier: CA378713267

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766957-C-A
• MyVariant Identifiers: chr10:g.131565221C>A (hg19) ; chr10:g.129766957C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766957C>A , CM000672.2:g.129766957C>A	GRCh38
NC_000010.10:g.131565221C>A , CM000672.1:g.131565221C>A	GRCh37
NC_000010.9:g.131455211C>A	NCBI36
NG_052673.1:g.304774C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.677C>A	ENSP00000302111.7:p.Ala226Glu
ENST00000651593.1:c.584C>A MANE Select	ENSP00000498729.1:p.Ala195Glu
ENST00000306010.7:c.677C>A	ENSP00000302111.7:p.Ala226Glu
NM_002412.3:c.677C>A	NP_002403.2:p.Ala226Glu
NM_002412.4:c.677C>A	NP_002403.2:p.Ala226Glu
XM_005252682.2:c.584C>A	XP_005252739.1:p.Ala195Glu
XM_006717863.2:c.407C>A	XP_006717926.1:p.Ala136Glu
XM_011539817.1:c.593C>A	XP_011538119.1:p.Ala198Glu
NM_002412.5:c.584C>A MANE Select	NP_002403.3:p.Ala195Glu
XM_017016275.1:c.407C>A	XP_016871764.1:p.Ala136Glu