Canonical Allele Identifier: CA2183422755
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029271G= , CM000677.2:g.65029271G= GRCh38
NC_000015.9:g.65321609G= , CM000677.1:g.65321609G= GRCh37
NC_000015.8:g.63108662G= NCBI36
NG_029184.1:g.5369C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+134C= MANE Select ENSP00000220058.4:n.209+134C=
ENST00000220058.8:c.209+134C= ENSP00000220058.4:n.209+134C=
ENST00000543678.1:c.209+134C= ENSP00000443754.1:n.209+134C=
ENST00000558460.5:c.209+134C= ENSP00000452646.1:n.209+134C=
ENST00000558614.1:n.170+134C=
ENST00000559633.1:n.128+134C=
ENST00000560717.5:c.194+134C= ENSP00000457257.1:n.194+134C=
NM_139242.3:c.209+134C= NP_640335.2:n.209+134C=
XM_005254158.3:c.-66C= XP_005254215.1:n.-66C=
XM_005254158.5:c.343C= XP_005254215.2:p.Arg115=
XR_001751081.1:n.358C=
NM_139242.4:c.209+134C= MANE Select NP_640335.2:n.209+134C=