Canonical Allele Identifier: CA2183422868
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029453C= , CM000677.2:g.65029453C= GRCh38
NC_000015.9:g.65321791C= , CM000677.1:g.65321791C= GRCh37
NC_000015.8:g.63108844C= NCBI36
NG_029184.1:g.5187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000220058.9:c.161G= MANE Select ENSP00000220058.4:p.Gly54=
ENST00000220058.8:c.161G= ENSP00000220058.4:p.Gly54=
ENST00000543678.1:c.161G= ENSP00000443754.1:p.Gly54=
ENST00000558460.5:c.161G= ENSP00000452646.1:p.Gly54=
ENST00000558614.1:n.122G=
ENST00000559633.1:n.80G=
ENST00000560717.5:c.146G= ENSP00000457257.1:p.Gly49=
NM_139242.3:c.161G= NP_640335.2:p.Gly54=
XM_005254158.5:c.161G= XP_005254215.2:p.Gly54=
XR_001751081.1:n.176G=
NM_139242.4:c.161G= MANE Select NP_640335.2:p.Gly54=