Canonical Allele Identifier: CA378713137

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565154G>A (hg19) ; chr10:g.129766890G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766890G>A , CM000672.2:g.129766890G>A	GRCh38
NC_000010.10:g.131565154G>A , CM000672.1:g.131565154G>A	GRCh37
NC_000010.9:g.131455144G>A	NCBI36
NG_052673.1:g.304707G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.610G>A	ENSP00000302111.7:p.Gly204Ser
ENST00000651593.1:c.517G>A MANE Select	ENSP00000498729.1:p.Gly173Ser
ENST00000306010.7:c.610G>A	ENSP00000302111.7:p.Gly204Ser
NM_002412.3:c.610G>A	NP_002403.2:p.Gly204Ser
NM_002412.4:c.610G>A	NP_002403.2:p.Gly204Ser
XM_005252682.2:c.517G>A	XP_005252739.1:p.Gly173Ser
XM_006717863.2:c.340G>A	XP_006717926.1:p.Gly114Ser
XM_011539817.1:c.526G>A	XP_011538119.1:p.Gly176Ser
NM_002412.5:c.517G>A MANE Select	NP_002403.3:p.Gly173Ser
XM_017016275.1:c.340G>A	XP_016871764.1:p.Gly114Ser