Canonical Allele Identifier: CA1944891250

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766938G= , CM000672.2:g.129766938G=	GRCh38
NC_000010.10:g.131565202G= , CM000672.1:g.131565202G=	GRCh37
NC_000010.9:g.131455192G=	NCBI36
NG_052673.1:g.304755G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.658G=	ENSP00000302111.7:p.Gly220=
ENST00000651593.1:c.565G= MANE Select	ENSP00000498729.1:p.Gly189=
ENST00000306010.7:c.658G=	ENSP00000302111.7:p.Gly220=
NM_002412.3:c.658G=	NP_002403.2:p.Gly220=
NM_002412.4:c.658G=	NP_002403.2:p.Gly220=
XM_005252682.2:c.565G=	XP_005252739.1:p.Gly189=
XM_006717863.2:c.388G=	XP_006717926.1:p.Gly130=
XM_011539817.1:c.574G=	XP_011538119.1:p.Gly192=
NM_002412.5:c.565G= MANE Select	NP_002403.3:p.Gly189=
XM_017016275.1:c.388G=	XP_016871764.1:p.Gly130=