Canonical Allele Identifier: CA2183422986
Gene: MTFMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029638C= , CM000677.2:g.65029638C= GRCh38
NC_000015.9:g.65321976C= , CM000677.1:g.65321976C= GRCh37
NC_000015.8:g.63109029C= NCBI36
NG_029184.1:g.5002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.-25G= MANE Select ENSP00000220058.4:n.-25G=
ENST00000543678.1:c.-25G= ENSP00000443754.1:n.-25G=
NM_139242.3:c.-25G= NP_640335.2:n.-25G=
NM_139242.4:c.-25G= MANE Select NP_640335.2:n.-25G=
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