Canonical Allele Identifier: CA1944891580
Gene: MGMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767156A= , CM000672.2:g.129767156A= GRCh38
NC_000010.10:g.131565420A= , CM000672.1:g.131565420A= GRCh37
NC_000010.9:g.131455410A= NCBI36
NG_052673.1:g.304973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*159A= ENSP00000302111.7:n.*159A=
ENST00000651593.1:c.*159A= MANE Select ENSP00000498729.1:n.*159A=
ENST00000306010.7:c.*159A= ENSP00000302111.7:n.*159A=
NM_002412.3:c.*159A= NP_002403.2:n.*159A=
NM_002412.4:c.*159A= NP_002403.2:n.*159A=
XM_006717863.2:c.*159A= XP_006717926.1:n.*159A=
XM_011539817.1:c.*159A= XP_011538119.1:n.*159A=
NM_002412.5:c.*159A= MANE Select NP_002403.3:n.*159A=
XM_017016275.1:c.*159A= XP_016871764.1:n.*159A=
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