Canonical Allele Identifier: CA2611438407
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767142_129767144del , CM000672.2:g.129767142_129767144del GRCh38
NC_000010.10:g.131565406_131565408del , CM000672.1:g.131565406_131565408del GRCh37
NC_000010.9:g.131455396_131455398del NCBI36
NG_052673.1:g.304959_304961del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*145_*147del ENSP00000302111.7:n.*145_*147del
ENST00000651593.1:c.*145_*147del MANE Select ENSP00000498729.1:n.*145_*147del
ENST00000306010.7:c.*145_*147del ENSP00000302111.7:n.*145_*147del
NM_002412.3:c.*145_*147del NP_002403.2:n.*145_*147del
NM_002412.4:c.*145_*147del NP_002403.2:n.*145_*147del
XM_006717863.2:c.*145_*147del XP_006717926.1:n.*145_*147del
XM_011539817.1:c.*145_*147del XP_011538119.1:n.*145_*147del
NM_002412.5:c.*145_*147del MANE Select NP_002403.3:n.*145_*147del
XM_017016275.1:c.*145_*147del XP_016871764.1:n.*145_*147del