Canonical Allele Identifier: CA1944891331

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766967C= , CM000672.2:g.129766967C=	GRCh38
NC_000010.10:g.131565231C= , CM000672.1:g.131565231C=	GRCh37
NC_000010.9:g.131455221C=	NCBI36
NG_052673.1:g.304784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.687C=	ENSP00000302111.7:p.Thr229=
ENST00000651593.1:c.594C= MANE Select	ENSP00000498729.1:p.Thr198=
ENST00000306010.7:c.687C=	ENSP00000302111.7:p.Thr229=
NM_002412.3:c.687C=	NP_002403.2:p.Thr229=
NM_002412.4:c.687C=	NP_002403.2:p.Thr229=
XM_005252682.2:c.594C=	XP_005252739.1:p.Thr198=
XM_006717863.2:c.417C=	XP_006717926.1:p.Thr139=
XM_011539817.1:c.603C=	XP_011538119.1:p.Thr201=
NM_002412.5:c.594C= MANE Select	NP_002403.3:p.Thr198=
XM_017016275.1:c.417C=	XP_016871764.1:p.Thr139=