Canonical Allele Identifier: CA1944891407

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766994C= , CM000672.2:g.129766994C=	GRCh38
NC_000010.10:g.131565258C= , CM000672.1:g.131565258C=	GRCh37
NC_000010.9:g.131455248C=	NCBI36
NG_052673.1:g.304811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.714C=	ENSP00000302111.7:p.Asn238=
ENST00000651593.1:c.621C= MANE Select	ENSP00000498729.1:p.Asn207=
ENST00000306010.7:c.714C=	ENSP00000302111.7:p.Asn238=
NM_002412.3:c.714C=	NP_002403.2:p.Asn238=
NM_002412.4:c.714C=	NP_002403.2:p.Asn238=
XM_005252682.2:c.621C=	XP_005252739.1:p.Asn207=
XM_006717863.2:c.444C=	XP_006717926.1:p.Asn148=
XM_011539817.1:c.630C=	XP_011538119.1:p.Asn210=
NM_002412.5:c.621C= MANE Select	NP_002403.3:p.Asn207=
XM_017016275.1:c.444C=	XP_016871764.1:p.Asn148=