Canonical Allele Identifier: CA1944822512
Gene: MGMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627797C= , CM000672.2:g.129627797C= GRCh38
NC_000010.10:g.131426061C= , CM000672.1:g.131426061C= GRCh37
NC_000010.9:g.131316051C= NCBI36
NG_052673.1:g.165614C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.219-80098C= ENSP00000302111.7:n.219-80098C=
ENST00000651593.1:c.126-80098C= MANE Select ENSP00000498729.1:n.126-80098C=
ENST00000306010.7:c.219-80098C= ENSP00000302111.7:n.219-80098C=
NM_002412.3:c.219-80098C= NP_002403.2:n.219-80098C=
NM_002412.4:c.219-80098C= NP_002403.2:n.219-80098C=
XM_005252682.2:c.126-80098C= XP_005252739.1:n.126-80098C=
XM_006717863.2:c.-125-18965C= XP_006717926.1:n.-125-18965C=
XM_011539817.1:c.-3-18965C= XP_011538119.1:n.-3-18965C=
NM_002412.5:c.126-80098C= MANE Select NP_002403.3:n.126-80098C=
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