Canonical Allele Identifier: CA1944921604
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766826C= , CM000672.2:g.129766826C= GRCh38
NC_000010.10:g.131565090C= , CM000672.1:g.131565090C= GRCh37
NC_000010.9:g.131455080C= NCBI36
NG_052673.1:g.304643C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.546C= ENSP00000302111.7:p.Ser182=
ENST00000651593.1:c.453C= MANE Select ENSP00000498729.1:p.Ser151=
ENST00000306010.7:c.546C= ENSP00000302111.7:p.Ser182=
NM_002412.3:c.546C= NP_002403.2:p.Ser182=
NM_002412.4:c.546C= NP_002403.2:p.Ser182=
XM_005252682.2:c.453C= XP_005252739.1:p.Ser151=
XM_006717863.2:c.276C= XP_006717926.1:p.Ser92=
XM_011539817.1:c.462C= XP_011538119.1:p.Ser154=
NM_002412.5:c.453C= MANE Select NP_002403.3:p.Ser151=
XM_017016275.1:c.276C= XP_016871764.1:p.Ser92=