Canonical Allele Identifier: CA1944891556
Gene: MGMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767128T= , CM000672.2:g.129767128T= GRCh38
NC_000010.10:g.131565392T= , CM000672.1:g.131565392T= GRCh37
NC_000010.9:g.131455382T= NCBI36
NG_052673.1:g.304945T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*131T= ENSP00000302111.7:n.*131T=
ENST00000651593.1:c.*131T= MANE Select ENSP00000498729.1:n.*131T=
ENST00000306010.7:c.*131T= ENSP00000302111.7:n.*131T=
NM_002412.3:c.*131T= NP_002403.2:n.*131T=
NM_002412.4:c.*131T= NP_002403.2:n.*131T=
XM_006717863.2:c.*131T= XP_006717926.1:n.*131T=
XM_011539817.1:c.*131T= XP_011538119.1:n.*131T=
NM_002412.5:c.*131T= MANE Select NP_002403.3:n.*131T=
XM_017016275.1:c.*131T= XP_016871764.1:n.*131T=
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