Canonical Allele Identifier: CA1944891382
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766987_129766988delinsGC , CM000672.2:g.129766987_129766988delinsGC GRCh38
NC_000010.10:g.131565251_131565252delinsGC , CM000672.1:g.131565251_131565252delinsGC GRCh37
NC_000010.9:g.131455241_131455242delinsGC NCBI36
NG_052673.1:g.304804_304805delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.707_708delinsGC ENSP00000302111.7:p.Gly236=
ENST00000651593.1:c.614_615delinsGC MANE Select ENSP00000498729.1:p.Gly205=
ENST00000306010.7:c.707_708delinsGC ENSP00000302111.7:p.Gly236=
NM_002412.3:c.707_708delinsGC NP_002403.2:p.Gly236=
NM_002412.4:c.707_708delinsGC NP_002403.2:p.Gly236=
XM_005252682.2:c.614_615delinsGC XP_005252739.1:p.Gly205=
XM_006717863.2:c.437_438delinsGC XP_006717926.1:p.Gly146=
XM_011539817.1:c.623_624delinsGC XP_011538119.1:p.Gly208=
NM_002412.5:c.614_615delinsGC MANE Select NP_002403.3:p.Gly205=
XM_017016275.1:c.437_438delinsGC XP_016871764.1:p.Gly146=