Canonical Allele Identifier: CA2513696561
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627767G>T , CM000672.2:g.129627767G>T GRCh38
NC_000010.10:g.131426031G>T , CM000672.1:g.131426031G>T GRCh37
NC_000010.9:g.131316021G>T NCBI36
NG_052673.1:g.165584G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.219-80128G>T ENSP00000302111.7:n.219-80128G>T
ENST00000651593.1:c.126-80128G>T MANE Select ENSP00000498729.1:n.126-80128G>T
ENST00000306010.7:c.219-80128G>T ENSP00000302111.7:n.219-80128G>T
NM_002412.3:c.219-80128G>T NP_002403.2:n.219-80128G>T
NM_002412.4:c.219-80128G>T NP_002403.2:n.219-80128G>T
XM_005252682.2:c.126-80128G>T XP_005252739.1:n.126-80128G>T
XM_006717863.2:c.-125-18995G>T XP_006717926.1:n.-125-18995G>T
XM_011539817.1:c.-3-18995G>T XP_011538119.1:n.-3-18995G>T
NM_002412.5:c.126-80128G>T MANE Select NP_002403.3:n.126-80128G>T