Canonical Allele Identifier: CA2183422838
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029401G= , CM000677.2:g.65029401G= GRCh38
NC_000015.9:g.65321739G= , CM000677.1:g.65321739G= GRCh37
NC_000015.8:g.63108792G= NCBI36
NG_029184.1:g.5239C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+4C= MANE Select ENSP00000220058.4:n.209+4C=
ENST00000220058.8:c.209+4C= ENSP00000220058.4:n.209+4C=
ENST00000543678.1:c.209+4C= ENSP00000443754.1:n.209+4C=
ENST00000558460.5:c.209+4C= ENSP00000452646.1:n.209+4C=
ENST00000558614.1:n.170+4C=
ENST00000559633.1:n.128+4C=
ENST00000560717.5:c.194+4C= ENSP00000457257.1:n.194+4C=
NM_139242.3:c.209+4C= NP_640335.2:n.209+4C=
XM_005254158.5:c.213C= XP_005254215.2:p.Tyr71=
XR_001751081.1:n.228C=
NM_139242.4:c.209+4C= MANE Select NP_640335.2:n.209+4C=