Canonical Allele Identifier: CA378713278
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766963C>T , CM000672.2:g.129766963C>T GRCh38
NC_000010.10:g.131565227C>T , CM000672.1:g.131565227C>T GRCh37
NC_000010.9:g.131455217C>T NCBI36
NG_052673.1:g.304780C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.683C>T ENSP00000302111.7:p.Ala228Val
ENST00000651593.1:c.590C>T MANE Select ENSP00000498729.1:p.Ala197Val
ENST00000306010.7:c.683C>T ENSP00000302111.7:p.Ala228Val
NM_002412.3:c.683C>T NP_002403.2:p.Ala228Val
NM_002412.4:c.683C>T NP_002403.2:p.Ala228Val
XM_005252682.2:c.590C>T XP_005252739.1:p.Ala197Val
XM_006717863.2:c.413C>T XP_006717926.1:p.Ala138Val
XM_011539817.1:c.599C>T XP_011538119.1:p.Ala200Val
NM_002412.5:c.590C>T MANE Select NP_002403.3:p.Ala197Val
XM_017016275.1:c.413C>T XP_016871764.1:p.Ala138Val