Canonical Allele Identifier: CA1944891267
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766945G= , CM000672.2:g.129766945G= GRCh38
NC_000010.10:g.131565209G= , CM000672.1:g.131565209G= GRCh37
NC_000010.9:g.131455199G= NCBI36
NG_052673.1:g.304762G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.665G= ENSP00000302111.7:p.Trp222=
ENST00000651593.1:c.572G= MANE Select ENSP00000498729.1:p.Trp191=
ENST00000306010.7:c.665G= ENSP00000302111.7:p.Trp222=
NM_002412.3:c.665G= NP_002403.2:p.Trp222=
NM_002412.4:c.665G= NP_002403.2:p.Trp222=
XM_005252682.2:c.572G= XP_005252739.1:p.Trp191=
XM_006717863.2:c.395G= XP_006717926.1:p.Trp132=
XM_011539817.1:c.581G= XP_011538119.1:p.Trp194=
NM_002412.5:c.572G= MANE Select NP_002403.3:p.Trp191=
XM_017016275.1:c.395G= XP_016871764.1:p.Trp132=