Canonical Allele Identifier: CA1944891212

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766915T= , CM000672.2:g.129766915T=	GRCh38
NC_000010.10:g.131565179T= , CM000672.1:g.131565179T=	GRCh37
NC_000010.9:g.131455169T=	NCBI36
NG_052673.1:g.304732T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.635T=	ENSP00000302111.7:p.Leu212=
ENST00000651593.1:c.542T= MANE Select	ENSP00000498729.1:p.Leu181=
ENST00000306010.7:c.635T=	ENSP00000302111.7:p.Leu212=
NM_002412.3:c.635T=	NP_002403.2:p.Leu212=
NM_002412.4:c.635T=	NP_002403.2:p.Leu212=
XM_005252682.2:c.542T=	XP_005252739.1:p.Leu181=
XM_006717863.2:c.365T=	XP_006717926.1:p.Leu122=
XM_011539817.1:c.551T=	XP_011538119.1:p.Leu184=
NM_002412.5:c.542T= MANE Select	NP_002403.3:p.Leu181=
XM_017016275.1:c.365T=	XP_016871764.1:p.Leu122=