Canonical Allele Identifier: CA2183422976
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029625C= , CM000677.2:g.65029625C= GRCh38
NC_000015.9:g.65321963C= , CM000677.1:g.65321963C= GRCh37
NC_000015.8:g.63109016C= NCBI36
NG_029184.1:g.5015G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.-12G= MANE Select ENSP00000220058.4:n.-12G=
ENST00000220058.8:c.-12G= ENSP00000220058.4:n.-12G=
ENST00000543678.1:c.-12G= ENSP00000443754.1:n.-12G=
NM_139242.3:c.-12G= NP_640335.2:n.-12G=
XM_005254158.5:c.-12G= XP_005254215.2:n.-12G=
XR_001751081.1:n.4G=
NM_139242.4:c.-12G= MANE Select NP_640335.2:n.-12G=