Canonical Allele Identifier: CA2611438316
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767033_129767034del , CM000672.2:g.129767033_129767034del GRCh38
NC_000010.10:g.131565297_131565298del , CM000672.1:g.131565297_131565298del GRCh37
NC_000010.9:g.131455287_131455288del NCBI36
NG_052673.1:g.304850_304851del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*36_*37del ENSP00000302111.7:n.*36_*37del
ENST00000651593.1:c.*36_*37del MANE Select ENSP00000498729.1:n.*36_*37del
ENST00000306010.7:c.*36_*37del ENSP00000302111.7:n.*36_*37del
NM_002412.3:c.*36_*37del NP_002403.2:n.*36_*37del
NM_002412.4:c.*36_*37del NP_002403.2:n.*36_*37del
XM_005252682.2:c.*36_*37del XP_005252739.1:n.*36_*37del
XM_006717863.2:c.*36_*37del XP_006717926.1:n.*36_*37del
XM_011539817.1:c.*36_*37del XP_011538119.1:n.*36_*37del
NM_002412.5:c.*36_*37del MANE Select NP_002403.3:n.*36_*37del
XM_017016275.1:c.*36_*37del XP_016871764.1:n.*36_*37del