Canonical Allele Identifier: CA1944760005
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467288T= , CM000672.2:g.129467288T= GRCh38
NC_000010.10:g.131265552T= , CM000672.1:g.131265552T= GRCh37
NC_000010.9:g.131155542T= NCBI36
NG_052673.1:g.5105T=

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.73T= ENSP00000302111.7:p.Cys25=
ENST00000651593.1:c.-21T= MANE Select ENSP00000498729.1:n.-21T=
ENST00000306010.7:c.73T= ENSP00000302111.7:p.Cys25=
ENST00000482547.1:n.27T=
ENST00000482653.1:n.60T=
NM_002412.3:c.73T= NP_002403.2:p.Cys25=
NM_002412.4:c.73T= NP_002403.2:p.Cys25=
NM_002412.5:c.-21T= MANE Select NP_002403.3:n.-21T=