Canonical Allele Identifier: CA2789967573
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767097C>G , CM000672.2:g.129767097C>G GRCh38
NC_000010.10:g.131565361C>G , CM000672.1:g.131565361C>G GRCh37
NC_000010.9:g.131455351C>G NCBI36
NG_052673.1:g.304914C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*100C>G ENSP00000302111.7:n.*100C>G
ENST00000651593.1:c.*100C>G MANE Select ENSP00000498729.1:n.*100C>G
ENST00000306010.7:c.*100C>G ENSP00000302111.7:n.*100C>G
NM_002412.3:c.*100C>G NP_002403.2:n.*100C>G
NM_002412.4:c.*100C>G NP_002403.2:n.*100C>G
XM_005252682.2:c.*100C>G XP_005252739.1:n.*100C>G
XM_006717863.2:c.*100C>G XP_006717926.1:n.*100C>G
XM_011539817.1:c.*100C>G XP_011538119.1:n.*100C>G
NM_002412.5:c.*100C>G MANE Select NP_002403.3:n.*100C>G
XM_017016275.1:c.*100C>G XP_016871764.1:n.*100C>G