Canonical Allele Identifier: CA2628983338

Gene: MTFMT

Linked Data

• gnomAD v4: 15-65029385-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029385C>A , CM000677.2:g.65029385C>A	GRCh38
NC_000015.9:g.65321723C>A , CM000677.1:g.65321723C>A	GRCh37
NC_000015.8:g.63108776C>A	NCBI36
NG_029184.1:g.5255G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.209+20G>T MANE Select	ENSP00000220058.4:n.209+20G>T
ENST00000220058.8:c.209+20G>T	ENSP00000220058.4:n.209+20G>T
ENST00000543678.1:c.209+20G>T	ENSP00000443754.1:n.209+20G>T
ENST00000558460.5:c.209+20G>T	ENSP00000452646.1:n.209+20G>T
ENST00000558614.1:n.170+20G>T
ENST00000559633.1:n.128+20G>T
ENST00000560717.5:c.194+20G>T	ENSP00000457257.1:n.194+20G>T
NM_139242.3:c.209+20G>T	NP_640335.2:n.209+20G>T
XM_005254158.5:c.229G>T	XP_005254215.2:p.Gly77Trp
XR_001751081.1:n.244G>T
NM_139242.4:c.209+20G>T MANE Select	NP_640335.2:n.209+20G>T