Canonical Allele Identifier: CA2580963670
Community Standard Title: NM_002412.5(MGMT):c.126-80137T>G
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627758T>G , CM000672.2:g.129627758T>G GRCh38
NC_000010.10:g.131426022T>G , CM000672.1:g.131426022T>G GRCh37
NC_000010.9:g.131316012T>G NCBI36
NG_052673.1:g.165575T>G

Transcript Alleles

HGVS Amino-acid Change
NM_002412.5:c.126-80137T>G MANE Select NP_002403.3:n.126-80137T>G
ENST00000651593.1:c.126-80137T>G MANE Select ENSP00000498729.1:n.126-80137T>G
NM_002412.3:c.219-80137T>G NP_002403.2:n.219-80137T>G
NM_002412.4:c.219-80137T>G NP_002403.2:n.219-80137T>G
ENST00000306010.7:c.219-80137T>G ENSP00000302111.7:n.219-80137T>G
ENST00000306010.8:c.219-80137T>G ENSP00000302111.7:n.219-80137T>G
XM_005252682.2:c.126-80137T>G XP_005252739.1:n.126-80137T>G
XM_006717863.2:c.-125-19004T>G XP_006717926.1:n.-125-19004T>G
XM_011539817.1:c.-3-19004T>G XP_011538119.1:n.-3-19004T>G