Canonical Allele Identifier: CA1944822507
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1847167412

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627787_129627790del , CM000672.2:g.129627787_129627790del GRCh38
NC_000010.10:g.131426051_131426054del , CM000672.1:g.131426051_131426054del GRCh37
NC_000010.9:g.131316041_131316044del NCBI36
NG_052673.1:g.165604_165607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.219-80108_219-80105del ENSP00000302111.7:n.219-80108_219-80105del
ENST00000651593.1:c.126-80108_126-80105del MANE Select ENSP00000498729.1:n.126-80108_126-80105del
ENST00000306010.7:c.219-80108_219-80105del ENSP00000302111.7:n.219-80108_219-80105del
NM_002412.3:c.219-80108_219-80105del NP_002403.2:n.219-80108_219-80105del
NM_002412.4:c.219-80108_219-80105del NP_002403.2:n.219-80108_219-80105del
XM_005252682.2:c.126-80108_126-80105del XP_005252739.1:n.126-80108_126-80105del
XM_006717863.2:c.-125-18975_-125-18972del XP_006717926.1:n.-125-18975_-125-18972del
XM_011539817.1:c.-3-18975_-3-18972del XP_011538119.1:n.-3-18975_-3-18972del
NM_002412.5:c.126-80108_126-80105del MANE Select NP_002403.3:n.126-80108_126-80105del