Canonical Allele Identifier: CA2574707798
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767026del , CM000672.2:g.129767026del GRCh38
NC_000010.10:g.131565290del , CM000672.1:g.131565290del GRCh37
NC_000010.9:g.131455280del NCBI36
NG_052673.1:g.304843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*29del ENSP00000302111.7:n.*29del
ENST00000651593.1:c.*29del MANE Select ENSP00000498729.1:n.*29del
ENST00000306010.7:c.*29del ENSP00000302111.7:n.*29del
NM_002412.3:c.*29del NP_002403.2:n.*29del
NM_002412.4:c.*29del NP_002403.2:n.*29del
XM_005252682.2:c.*29del XP_005252739.1:n.*29del
XM_006717863.2:c.*29del XP_006717926.1:n.*29del
XM_011539817.1:c.*29del XP_011538119.1:n.*29del
NM_002412.5:c.*29del MANE Select NP_002403.3:n.*29del
XM_017016275.1:c.*29del XP_016871764.1:n.*29del