Canonical Allele Identifier: CA1944891537
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767099_129767100delinsTG , CM000672.2:g.129767099_129767100delinsTG GRCh38
NC_000010.10:g.131565363_131565364delinsTG , CM000672.1:g.131565363_131565364delinsTG GRCh37
NC_000010.9:g.131455353_131455354delinsTG NCBI36
NG_052673.1:g.304916_304917delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*102_*103delinsTG ENSP00000302111.7:n.*102_*103delinsTG
ENST00000651593.1:c.*102_*103delinsTG MANE Select ENSP00000498729.1:n.*102_*103delinsTG
ENST00000306010.7:c.*102_*103delinsTG ENSP00000302111.7:n.*102_*103delinsTG
NM_002412.3:c.*102_*103delinsTG NP_002403.2:n.*102_*103delinsTG
NM_002412.4:c.*102_*103delinsTG NP_002403.2:n.*102_*103delinsTG
XM_005252682.2:c.*102_*103delinsTG XP_005252739.1:n.*102_*103delinsTG
XM_006717863.2:c.*102_*103delinsTG XP_006717926.1:n.*102_*103delinsTG
XM_011539817.1:c.*102_*103delinsTG XP_011538119.1:n.*102_*103delinsTG
NM_002412.5:c.*102_*103delinsTG MANE Select NP_002403.3:n.*102_*103delinsTG
XM_017016275.1:c.*102_*103delinsTG XP_016871764.1:n.*102_*103delinsTG