Canonical Allele Identifier: CA471816701

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766991-A-G
• MyVariant Identifiers: chr10:g.131565255A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766991A>G , CM000672.2:g.129766991A>G	GRCh38
NC_000010.10:g.131565255A>G , CM000672.1:g.131565255A>G	GRCh37
NC_000010.9:g.131455245A>G	NCBI36
NG_052673.1:g.304808A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.711A>G	ENSP00000302111.7:p.Arg237=
ENST00000651593.1:c.618A>G MANE Select	ENSP00000498729.1:p.Arg206=
ENST00000306010.7:c.711A>G	ENSP00000302111.7:p.Arg237=
NM_002412.3:c.711A>G	NP_002403.2:p.Arg237=
NM_002412.4:c.711A>G	NP_002403.2:p.Arg237=
XM_005252682.2:c.618A>G	XP_005252739.1:p.Arg206=
XM_006717863.2:c.441A>G	XP_006717926.1:p.Arg147=
XM_011539817.1:c.627A>G	XP_011538119.1:p.Arg209=
NM_002412.5:c.618A>G MANE Select	NP_002403.3:p.Arg206=
XM_017016275.1:c.441A>G	XP_016871764.1:p.Arg147=