Canonical Allele Identifier: CA2611438404
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767137del , CM000672.2:g.129767137del GRCh38
NC_000010.10:g.131565401del , CM000672.1:g.131565401del GRCh37
NC_000010.9:g.131455391del NCBI36
NG_052673.1:g.304954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*140del ENSP00000302111.7:n.*140del
ENST00000651593.1:c.*140del MANE Select ENSP00000498729.1:n.*140del
ENST00000306010.7:c.*140del ENSP00000302111.7:n.*140del
NM_002412.3:c.*140del NP_002403.2:n.*140del
NM_002412.4:c.*140del NP_002403.2:n.*140del
XM_006717863.2:c.*140del XP_006717926.1:n.*140del
XM_011539817.1:c.*140del XP_011538119.1:n.*140del
NM_002412.5:c.*140del MANE Select NP_002403.3:n.*140del
XM_017016275.1:c.*140del XP_016871764.1:n.*140del