Canonical Allele Identifier: CA392863862
Gene: MTFMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029603A>T , CM000677.2:g.65029603A>T GRCh38
NC_000015.9:g.65321941A>T , CM000677.1:g.65321941A>T GRCh37
NC_000015.8:g.63108994A>T NCBI36
NG_029184.1:g.5037T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.11T>A MANE Select ENSP00000220058.4:p.Leu4Ter
ENST00000220058.8:c.11T>A ENSP00000220058.4:p.Leu4Ter
ENST00000543678.1:c.11T>A ENSP00000443754.1:p.Leu4Ter
ENST00000558460.5:c.11T>A ENSP00000452646.1:p.Leu4Ter
NM_139242.3:c.11T>A NP_640335.2:p.Leu4Ter
XM_005254158.5:c.11T>A XP_005254215.2:p.Leu4Ter
XR_001751081.1:n.26T>A
NM_139242.4:c.11T>A MANE Select NP_640335.2:p.Leu4Ter