Canonical Allele Identifier: CA1944891547
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767115_129767117delinsTGC , CM000672.2:g.129767115_129767117delinsTGC GRCh38
NC_000010.10:g.131565379_131565381delinsTGC , CM000672.1:g.131565379_131565381delinsTGC GRCh37
NC_000010.9:g.131455369_131455371delinsTGC NCBI36
NG_052673.1:g.304932_304934delinsTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*118_*120delinsTGC ENSP00000302111.7:n.*118_*120delinsTGC
ENST00000651593.1:c.*118_*120delinsTGC MANE Select ENSP00000498729.1:n.*118_*120delinsTGC
ENST00000306010.7:c.*118_*120delinsTGC ENSP00000302111.7:n.*118_*120delinsTGC
NM_002412.3:c.*118_*120delinsTGC NP_002403.2:n.*118_*120delinsTGC
NM_002412.4:c.*118_*120delinsTGC NP_002403.2:n.*118_*120delinsTGC
XM_006717863.2:c.*118_*120delinsTGC XP_006717926.1:n.*118_*120delinsTGC
XM_011539817.1:c.*118_*120delinsTGC XP_011538119.1:n.*118_*120delinsTGC
NM_002412.5:c.*118_*120delinsTGC MANE Select NP_002403.3:n.*118_*120delinsTGC
XM_017016275.1:c.*118_*120delinsTGC XP_016871764.1:n.*118_*120delinsTGC