Canonical Allele Identifier: CA378713318

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565250G>C (hg19) ; chr10:g.129766986G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766986G>C , CM000672.2:g.129766986G>C	GRCh38
NC_000010.10:g.131565250G>C , CM000672.1:g.131565250G>C	GRCh37
NC_000010.9:g.131455240G>C	NCBI36
NG_052673.1:g.304803G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.706G>C	ENSP00000302111.7:p.Gly236Arg
ENST00000651593.1:c.613G>C MANE Select	ENSP00000498729.1:p.Gly205Arg
ENST00000306010.7:c.706G>C	ENSP00000302111.7:p.Gly236Arg
NM_002412.3:c.706G>C	NP_002403.2:p.Gly236Arg
NM_002412.4:c.706G>C	NP_002403.2:p.Gly236Arg
XM_005252682.2:c.613G>C	XP_005252739.1:p.Gly205Arg
XM_006717863.2:c.436G>C	XP_006717926.1:p.Gly146Arg
XM_011539817.1:c.622G>C	XP_011538119.1:p.Gly208Arg
NM_002412.5:c.613G>C MANE Select	NP_002403.3:p.Gly205Arg
XM_017016275.1:c.436G>C	XP_016871764.1:p.Gly146Arg