Canonical Allele Identifier: CA1944921617
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766854G= , CM000672.2:g.129766854G= GRCh38
NC_000010.10:g.131565118G= , CM000672.1:g.131565118G= GRCh37
NC_000010.9:g.131455108G= NCBI36
NG_052673.1:g.304671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.574G= ENSP00000302111.7:p.Gly192=
ENST00000651593.1:c.481G= MANE Select ENSP00000498729.1:p.Gly161=
ENST00000306010.7:c.574G= ENSP00000302111.7:p.Gly192=
NM_002412.3:c.574G= NP_002403.2:p.Gly192=
NM_002412.4:c.574G= NP_002403.2:p.Gly192=
XM_005252682.2:c.481G= XP_005252739.1:p.Gly161=
XM_006717863.2:c.304G= XP_006717926.1:p.Gly102=
XM_011539817.1:c.490G= XP_011538119.1:p.Gly164=
NM_002412.5:c.481G= MANE Select NP_002403.3:p.Gly161=
XM_017016275.1:c.304G= XP_016871764.1:p.Gly102=