Canonical Allele Identifier: CA2804503427
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029316A>T , CM000677.2:g.65029316A>T GRCh38
NC_000015.9:g.65321654A>T , CM000677.1:g.65321654A>T GRCh37
NC_000015.8:g.63108707A>T NCBI36
NG_029184.1:g.5324T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+89T>A MANE Select ENSP00000220058.4:n.209+89T>A
ENST00000220058.8:c.209+89T>A ENSP00000220058.4:n.209+89T>A
ENST00000543678.1:c.209+89T>A ENSP00000443754.1:n.209+89T>A
ENST00000558460.5:c.209+89T>A ENSP00000452646.1:n.209+89T>A
ENST00000558614.1:n.170+89T>A
ENST00000559633.1:n.128+89T>A
ENST00000560717.5:c.194+89T>A ENSP00000457257.1:n.194+89T>A
NM_139242.3:c.209+89T>A NP_640335.2:n.209+89T>A
XM_005254158.3:c.-111T>A XP_005254215.1:n.-111T>A
XM_005254158.5:c.298T>A XP_005254215.2:p.Leu100Met
XR_001751081.1:n.313T>A
NM_139242.4:c.209+89T>A MANE Select NP_640335.2:n.209+89T>A