Canonical Allele Identifier: CA1944891450
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767012A= , CM000672.2:g.129767012A= GRCh38
NC_000010.10:g.131565276A= , CM000672.1:g.131565276A= GRCh37
NC_000010.9:g.131455266A= NCBI36
NG_052673.1:g.304829A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*15A= ENSP00000302111.7:n.*15A=
ENST00000651593.1:c.*15A= MANE Select ENSP00000498729.1:n.*15A=
ENST00000306010.7:c.*15A= ENSP00000302111.7:n.*15A=
NM_002412.3:c.*15A= NP_002403.2:n.*15A=
NM_002412.4:c.*15A= NP_002403.2:n.*15A=
XM_005252682.2:c.*15A= XP_005252739.1:n.*15A=
XM_006717863.2:c.*15A= XP_006717926.1:n.*15A=
XM_011539817.1:c.*15A= XP_011538119.1:n.*15A=
NM_002412.5:c.*15A= MANE Select NP_002403.3:n.*15A=
XM_017016275.1:c.*15A= XP_016871764.1:n.*15A=