Canonical Allele Identifier: CA1944822481
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627762C= , CM000672.2:g.129627762C= GRCh38
NC_000010.10:g.131426026C= , CM000672.1:g.131426026C= GRCh37
NC_000010.9:g.131316016C= NCBI36
NG_052673.1:g.165579C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.219-80133C= ENSP00000302111.7:n.219-80133C=
ENST00000651593.1:c.126-80133C= MANE Select ENSP00000498729.1:n.126-80133C=
ENST00000306010.7:c.219-80133C= ENSP00000302111.7:n.219-80133C=
NM_002412.3:c.219-80133C= NP_002403.2:n.219-80133C=
NM_002412.4:c.219-80133C= NP_002403.2:n.219-80133C=
XM_005252682.2:c.126-80133C= XP_005252739.1:n.126-80133C=
XM_006717863.2:c.-125-19000C= XP_006717926.1:n.-125-19000C=
XM_011539817.1:c.-3-19000C= XP_011538119.1:n.-3-19000C=
NM_002412.5:c.126-80133C= MANE Select NP_002403.3:n.126-80133C=