Canonical Allele Identifier: CA1944891485
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767039_129767041delinsAAC , CM000672.2:g.129767039_129767041delinsAAC GRCh38
NC_000010.10:g.131565303_131565305delinsAAC , CM000672.1:g.131565303_131565305delinsAAC GRCh37
NC_000010.9:g.131455293_131455295delinsAAC NCBI36
NG_052673.1:g.304856_304858delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*42_*44delinsAAC ENSP00000302111.7:n.*42_*44delinsAAC
ENST00000651593.1:c.*42_*44delinsAAC MANE Select ENSP00000498729.1:n.*42_*44delinsAAC
ENST00000306010.7:c.*42_*44delinsAAC ENSP00000302111.7:n.*42_*44delinsAAC
NM_002412.3:c.*42_*44delinsAAC NP_002403.2:n.*42_*44delinsAAC
NM_002412.4:c.*42_*44delinsAAC NP_002403.2:n.*42_*44delinsAAC
XM_005252682.2:c.*42_*44delinsAAC XP_005252739.1:n.*42_*44delinsAAC
XM_006717863.2:c.*42_*44delinsAAC XP_006717926.1:n.*42_*44delinsAAC
XM_011539817.1:c.*42_*44delinsAAC XP_011538119.1:n.*42_*44delinsAAC
NM_002412.5:c.*42_*44delinsAAC MANE Select NP_002403.3:n.*42_*44delinsAAC
XM_017016275.1:c.*42_*44delinsAAC XP_016871764.1:n.*42_*44delinsAAC