Canonical Allele Identifier: CA1944891514
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767061G= , CM000672.2:g.129767061G= GRCh38
NC_000010.10:g.131565325G= , CM000672.1:g.131565325G= GRCh37
NC_000010.9:g.131455315G= NCBI36
NG_052673.1:g.304878G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*64G= ENSP00000302111.7:n.*64G=
ENST00000651593.1:c.*64G= MANE Select ENSP00000498729.1:n.*64G=
ENST00000306010.7:c.*64G= ENSP00000302111.7:n.*64G=
NM_002412.3:c.*64G= NP_002403.2:n.*64G=
NM_002412.4:c.*64G= NP_002403.2:n.*64G=
XM_005252682.2:c.*64G= XP_005252739.1:n.*64G=
XM_006717863.2:c.*64G= XP_006717926.1:n.*64G=
XM_011539817.1:c.*64G= XP_011538119.1:n.*64G=
NM_002412.5:c.*64G= MANE Select NP_002403.3:n.*64G=
XM_017016275.1:c.*64G= XP_016871764.1:n.*64G=