Canonical Allele Identifier: CA1944891589
Gene: MGMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767161C= , CM000672.2:g.129767161C= GRCh38
NC_000010.10:g.131565425C= , CM000672.1:g.131565425C= GRCh37
NC_000010.9:g.131455415C= NCBI36
NG_052673.1:g.304978C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*164C= ENSP00000302111.7:n.*164C=
ENST00000651593.1:c.*164C= MANE Select ENSP00000498729.1:n.*164C=
ENST00000306010.7:c.*164C= ENSP00000302111.7:n.*164C=
NM_002412.3:c.*164C= NP_002403.2:n.*164C=
NM_002412.4:c.*164C= NP_002403.2:n.*164C=
XM_006717863.2:c.*164C= XP_006717926.1:n.*164C=
XM_011539817.1:c.*164C= XP_011538119.1:n.*164C=
NM_002412.5:c.*164C= MANE Select NP_002403.3:n.*164C=
XM_017016275.1:c.*164C= XP_016871764.1:n.*164C=
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