Canonical Allele Identifier: CA378713121

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766882-C-G
• MyVariant Identifiers: chr10:g.131565146C>G (hg19) ; chr10:g.129766882C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766882C>G , CM000672.2:g.129766882C>G	GRCh38
NC_000010.10:g.131565146C>G , CM000672.1:g.131565146C>G	GRCh37
NC_000010.9:g.131455136C>G	NCBI36
NG_052673.1:g.304699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.602C>G	ENSP00000302111.7:p.Ala201Gly
ENST00000651593.1:c.509C>G MANE Select	ENSP00000498729.1:p.Ala170Gly
ENST00000306010.7:c.602C>G	ENSP00000302111.7:p.Ala201Gly
NM_002412.3:c.602C>G	NP_002403.2:p.Ala201Gly
NM_002412.4:c.602C>G	NP_002403.2:p.Ala201Gly
XM_005252682.2:c.509C>G	XP_005252739.1:p.Ala170Gly
XM_006717863.2:c.332C>G	XP_006717926.1:p.Ala111Gly
XM_011539817.1:c.518C>G	XP_011538119.1:p.Ala173Gly
NM_002412.5:c.509C>G MANE Select	NP_002403.3:p.Ala170Gly
XM_017016275.1:c.332C>G	XP_016871764.1:p.Ala111Gly