Canonical Allele Identifier: CA1944877122

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129676210G= , CM000672.2:g.129676210G=	GRCh38
NC_000010.10:g.131474474G= , CM000672.1:g.131474474G=	GRCh37
NC_000010.9:g.131364464G=	NCBI36
NG_052673.1:g.214027G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002412.5:c.126-31685G= MANE Select	NP_002403.3:n.126-31685G=
ENST00000651593.1:c.126-31685G= MANE Select	ENSP00000498729.1:n.126-31685G=
NM_002412.3:c.219-31685G=	NP_002403.2:n.219-31685G=
NM_002412.4:c.219-31685G=	NP_002403.2:n.219-31685G=
ENST00000306010.7:c.219-31685G=	ENSP00000302111.7:n.219-31685G=
ENST00000306010.8:c.219-31685G=	ENSP00000302111.7:n.219-31685G=
XM_005252682.2:c.126-31685G=	XP_005252739.1:n.126-31685G=
XM_006717863.2:c.-53+29376G=	XP_006717926.1:n.-53+29376G=
XM_011539817.1:c.134+29312G=	XP_011538119.1:n.134+29312G=
XM_017016275.1:c.-53+29376G=	XP_016871764.1:n.-53+29376G=