Canonical Allele Identifier: CA1944822455
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627731T= , CM000672.2:g.129627731T= GRCh38
NC_000010.10:g.131425995T= , CM000672.1:g.131425995T= GRCh37
NC_000010.9:g.131315985T= NCBI36
NG_052673.1:g.165548T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.219-80164T= ENSP00000302111.7:n.219-80164T=
ENST00000651593.1:c.126-80164T= MANE Select ENSP00000498729.1:n.126-80164T=
ENST00000306010.7:c.219-80164T= ENSP00000302111.7:n.219-80164T=
NM_002412.3:c.219-80164T= NP_002403.2:n.219-80164T=
NM_002412.4:c.219-80164T= NP_002403.2:n.219-80164T=
XM_005252682.2:c.126-80164T= XP_005252739.1:n.126-80164T=
XM_006717863.2:c.-125-19031T= XP_006717926.1:n.-125-19031T=
XM_011539817.1:c.-3-19031T= XP_011538119.1:n.-3-19031T=
NM_002412.5:c.126-80164T= MANE Select NP_002403.3:n.126-80164T=