Canonical Allele Identifier: CA1944891369

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766980C= , CM000672.2:g.129766980C=	GRCh38
NC_000010.10:g.131565244C= , CM000672.1:g.131565244C=	GRCh37
NC_000010.9:g.131455234C=	NCBI36
NG_052673.1:g.304797C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.700C=	ENSP00000302111.7:p.Pro234=
ENST00000651593.1:c.607C= MANE Select	ENSP00000498729.1:p.Pro203=
ENST00000306010.7:c.700C=	ENSP00000302111.7:p.Pro234=
NM_002412.3:c.700C=	NP_002403.2:p.Pro234=
NM_002412.4:c.700C=	NP_002403.2:p.Pro234=
XM_005252682.2:c.607C=	XP_005252739.1:p.Pro203=
XM_006717863.2:c.430C=	XP_006717926.1:p.Pro144=
XM_011539817.1:c.616C=	XP_011538119.1:p.Pro206=
NM_002412.5:c.607C= MANE Select	NP_002403.3:p.Pro203=
XM_017016275.1:c.430C=	XP_016871764.1:p.Pro144=