Canonical Allele Identifier: CA2575758833
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029206C>A , CM000677.2:g.65029206C>A GRCh38
NC_000015.9:g.65321544C>A , CM000677.1:g.65321544C>A GRCh37
NC_000015.8:g.63108597C>A NCBI36
NG_029184.1:g.5434G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+199G>T MANE Select ENSP00000220058.4:n.209+199G>T
ENST00000220058.8:c.209+199G>T ENSP00000220058.4:n.209+199G>T
ENST00000543678.1:c.209+199G>T ENSP00000443754.1:n.209+199G>T
ENST00000558460.5:c.209+199G>T ENSP00000452646.1:n.209+199G>T
ENST00000558614.1:n.170+199G>T
ENST00000559633.1:n.128+199G>T
ENST00000560717.5:c.194+199G>T ENSP00000457257.1:n.194+199G>T
NM_139242.3:c.209+199G>T NP_640335.2:n.209+199G>T
XM_005254158.3:c.-47+46G>T XP_005254215.1:n.-47+46G>T
XM_005254158.5:c.362+46G>T XP_005254215.2:n.362+46G>T
XR_001751081.1:n.377+46G>T
NM_139242.4:c.209+199G>T MANE Select NP_640335.2:n.209+199G>T