Canonical Allele Identifier: CA2570229544
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029269A>T , CM000677.2:g.65029269A>T GRCh38
NC_000015.9:g.65321607A>T , CM000677.1:g.65321607A>T GRCh37
NC_000015.8:g.63108660A>T NCBI36
NG_029184.1:g.5371T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+136T>A MANE Select ENSP00000220058.4:n.209+136T>A
ENST00000220058.8:c.209+136T>A ENSP00000220058.4:n.209+136T>A
ENST00000543678.1:c.209+136T>A ENSP00000443754.1:n.209+136T>A
ENST00000558460.5:c.209+136T>A ENSP00000452646.1:n.209+136T>A
ENST00000558614.1:n.170+136T>A
ENST00000559633.1:n.128+136T>A
ENST00000560717.5:c.194+136T>A ENSP00000457257.1:n.194+136T>A
NM_139242.3:c.209+136T>A NP_640335.2:n.209+136T>A
XM_005254158.3:c.-64T>A XP_005254215.1:n.-64T>A
XM_005254158.5:c.345T>A XP_005254215.2:p.Arg115=
XR_001751081.1:n.360T>A
NM_139242.4:c.209+136T>A MANE Select NP_640335.2:n.209+136T>A