Canonical Allele Identifier: CA392863273
Gene: MTFMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029547T>A , CM000677.2:g.65029547T>A GRCh38
NC_000015.9:g.65321885T>A , CM000677.1:g.65321885T>A GRCh37
NC_000015.8:g.63108938T>A NCBI36
NG_029184.1:g.5093A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000220058.9:c.67A>T MANE Select ENSP00000220058.4:p.Ser23Cys
ENST00000220058.8:c.67A>T ENSP00000220058.4:p.Ser23Cys
ENST00000543678.1:c.67A>T ENSP00000443754.1:p.Ser23Cys
ENST00000558460.5:c.67A>T ENSP00000452646.1:p.Ser23Cys
ENST00000558614.1:n.28A>T
ENST00000560717.5:c.52A>T ENSP00000457257.1:p.Ser18Cys
NM_139242.3:c.67A>T NP_640335.2:p.Ser23Cys
XM_005254158.5:c.67A>T XP_005254215.2:p.Ser23Cys
XR_001751081.1:n.82A>T
NM_139242.4:c.67A>T MANE Select NP_640335.2:p.Ser23Cys