Canonical Allele Identifier: CA1944870565

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129711417G= , CM000672.2:g.129711417G=	GRCh38
NC_000010.10:g.131509681G= , CM000672.1:g.131509681G=	GRCh37
NC_000010.9:g.131399671G=	NCBI36
NG_052673.1:g.249234G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002412.5:c.274+3374G= MANE Select	NP_002403.3:n.274+3374G=
ENST00000651593.1:c.274+3374G= MANE Select	ENSP00000498729.1:n.274+3374G=
NM_002412.3:c.367+3374G=	NP_002403.2:n.367+3374G=
NM_002412.4:c.367+3374G=	NP_002403.2:n.367+3374G=
ENST00000306010.7:c.367+3374G=	ENSP00000302111.7:n.367+3374G=
ENST00000306010.8:c.367+3374G=	ENSP00000302111.7:n.367+3374G=
ENST00000462672.1:n.435+3374G=
XM_005252682.2:c.274+3374G=	XP_005252739.1:n.274+3374G=
XM_006717863.2:c.97+3374G=	XP_006717926.1:n.97+3374G=
XM_011539817.1:c.283+3374G=	XP_011538119.1:n.283+3374G=
XM_017016275.1:c.97+3374G=	XP_016871764.1:n.97+3374G=
XR_946467.2:n.3368G=