Canonical Allele Identifier: CA1944891186
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766906A= , CM000672.2:g.129766906A= GRCh38
NC_000010.10:g.131565170A= , CM000672.1:g.131565170A= GRCh37
NC_000010.9:g.131455160A= NCBI36
NG_052673.1:g.304723A=

Transcript Alleles

HGVS Amino-acid Change
NM_002412.5:c.533A= MANE Select NP_002403.3:p.Lys178=
ENST00000651593.1:c.533A= MANE Select ENSP00000498729.1:p.Lys178=
NM_002412.3:c.626A= NP_002403.2:p.Lys209=
NM_002412.4:c.626A= NP_002403.2:p.Lys209=
ENST00000306010.7:c.626A= ENSP00000302111.7:p.Lys209=
ENST00000306010.8:c.626A= ENSP00000302111.7:p.Lys209=
XM_005252682.2:c.533A= XP_005252739.1:p.Lys178=
XM_006717863.2:c.356A= XP_006717926.1:p.Lys119=
XM_011539817.1:c.542A= XP_011538119.1:p.Lys181=
XM_017016275.1:c.356A= XP_016871764.1:p.Lys119=