Canonical Allele Identifier: CA471816578

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565160C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766896C>A , CM000672.2:g.129766896C>A	GRCh38
NC_000010.10:g.131565160C>A , CM000672.1:g.131565160C>A	GRCh37
NC_000010.9:g.131455150C>A	NCBI36
NG_052673.1:g.304713C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.616C>A	ENSP00000302111.7:p.Arg206=
ENST00000651593.1:c.523C>A MANE Select	ENSP00000498729.1:p.Arg175=
ENST00000306010.7:c.616C>A	ENSP00000302111.7:p.Arg206=
NM_002412.3:c.616C>A	NP_002403.2:p.Arg206=
NM_002412.4:c.616C>A	NP_002403.2:p.Arg206=
XM_005252682.2:c.523C>A	XP_005252739.1:p.Arg175=
XM_006717863.2:c.346C>A	XP_006717926.1:p.Arg116=
XM_011539817.1:c.532C>A	XP_011538119.1:p.Arg178=
NM_002412.5:c.523C>A MANE Select	NP_002403.3:p.Arg175=
XM_017016275.1:c.346C>A	XP_016871764.1:p.Arg116=