Canonical Allele Identifier: CA1944760499
Gene: MGMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129468170C= , CM000672.2:g.129468170C= GRCh38
NC_000010.10:g.131266434C= , CM000672.1:g.131266434C= GRCh37
NC_000010.9:g.131156424C= NCBI36
NG_052673.1:g.5987C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.81+874C= ENSP00000302111.7:n.81+874C=
ENST00000651593.1:c.-13+874C= MANE Select ENSP00000498729.1:n.-13+874C=
ENST00000306010.7:c.81+874C= ENSP00000302111.7:n.81+874C=
ENST00000482547.1:n.35+874C=
ENST00000482653.1:n.68+874C=
NM_002412.3:c.81+874C= NP_002403.2:n.81+874C=
NM_002412.4:c.81+874C= NP_002403.2:n.81+874C=
XM_005252682.2:c.-13+729C= XP_005252739.1:n.-13+729C=
NM_002412.5:c.-13+874C= MANE Select NP_002403.3:n.-13+874C=
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