Canonical Allele Identifier: CA2628983314
Gene: MTFMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029369T>A , CM000677.2:g.65029369T>A GRCh38
NC_000015.9:g.65321707T>A , CM000677.1:g.65321707T>A GRCh37
NC_000015.8:g.63108760T>A NCBI36
NG_029184.1:g.5271A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+36A>T MANE Select ENSP00000220058.4:n.209+36A>T
ENST00000220058.8:c.209+36A>T ENSP00000220058.4:n.209+36A>T
ENST00000543678.1:c.209+36A>T ENSP00000443754.1:n.209+36A>T
ENST00000558460.5:c.209+36A>T ENSP00000452646.1:n.209+36A>T
ENST00000558614.1:n.170+36A>T
ENST00000559633.1:n.128+36A>T
ENST00000560717.5:c.194+36A>T ENSP00000457257.1:n.194+36A>T
NM_139242.3:c.209+36A>T NP_640335.2:n.209+36A>T
XM_005254158.5:c.245A>T XP_005254215.2:p.Glu82Val
XR_001751081.1:n.260A>T
NM_139242.4:c.209+36A>T MANE Select NP_640335.2:n.209+36A>T