Canonical Allele Identifier: CA1944891459

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767028C= , CM000672.2:g.129767028C=	GRCh38
NC_000010.10:g.131565292C= , CM000672.1:g.131565292C=	GRCh37
NC_000010.9:g.131455282C=	NCBI36
NG_052673.1:g.304845C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*31C=	ENSP00000302111.7:n.*31C=
ENST00000651593.1:c.*31C= MANE Select	ENSP00000498729.1:n.*31C=
ENST00000306010.7:c.*31C=	ENSP00000302111.7:n.*31C=
NM_002412.3:c.*31C=	NP_002403.2:n.*31C=
NM_002412.4:c.*31C=	NP_002403.2:n.*31C=
XM_005252682.2:c.*31C=	XP_005252739.1:n.*31C=
XM_006717863.2:c.*31C=	XP_006717926.1:n.*31C=
XM_011539817.1:c.*31C=	XP_011538119.1:n.*31C=
NM_002412.5:c.*31C= MANE Select	NP_002403.3:n.*31C=
XM_017016275.1:c.*31C=	XP_016871764.1:n.*31C=