Canonical Allele Identifier: CA378713311

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766983-G-C
• MyVariant Identifiers: chr10:g.131565247G>C (hg19) ; chr10:g.129766983G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766983G>C , CM000672.2:g.129766983G>C	GRCh38
NC_000010.10:g.131565247G>C , CM000672.1:g.131565247G>C	GRCh37
NC_000010.9:g.131455237G>C	NCBI36
NG_052673.1:g.304800G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.703G>C	ENSP00000302111.7:p.Ala235Pro
ENST00000651593.1:c.610G>C MANE Select	ENSP00000498729.1:p.Ala204Pro
ENST00000306010.7:c.703G>C	ENSP00000302111.7:p.Ala235Pro
NM_002412.3:c.703G>C	NP_002403.2:p.Ala235Pro
NM_002412.4:c.703G>C	NP_002403.2:p.Ala235Pro
XM_005252682.2:c.610G>C	XP_005252739.1:p.Ala204Pro
XM_006717863.2:c.433G>C	XP_006717926.1:p.Ala145Pro
XM_011539817.1:c.619G>C	XP_011538119.1:p.Ala207Pro
NM_002412.5:c.610G>C MANE Select	NP_002403.3:p.Ala204Pro
XM_017016275.1:c.433G>C	XP_016871764.1:p.Ala145Pro