Canonical Allele Identifier: CA2628983214
Gene: MTFMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029215del , CM000677.2:g.65029215del GRCh38
NC_000015.9:g.65321553del , CM000677.1:g.65321553del GRCh37
NC_000015.8:g.63108606del NCBI36
NG_029184.1:g.5425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+190del MANE Select ENSP00000220058.4:n.209+190del
ENST00000220058.8:c.209+190del ENSP00000220058.4:n.209+190del
ENST00000543678.1:c.209+190del ENSP00000443754.1:n.209+190del
ENST00000558460.5:c.209+190del ENSP00000452646.1:n.209+190del
ENST00000558614.1:n.170+190del
ENST00000559633.1:n.128+190del
ENST00000560717.5:c.194+190del ENSP00000457257.1:n.194+190del
NM_139242.3:c.209+190del NP_640335.2:n.209+190del
XM_005254158.3:c.-47+37del XP_005254215.1:n.-47+37del
XM_005254158.5:c.362+37del XP_005254215.2:n.362+37del
XR_001751081.1:n.377+37del
NM_139242.4:c.209+190del MANE Select NP_640335.2:n.209+190del