Canonical Allele Identifier: CA392862017
Gene: MTFMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1351160
ClinVar RCV Id: RCV002044521
dbSNP Id: rs1264914031
gnomAD v2: 15-65321758-G-A
gnomAD v4: 15-65029420-G-A
MyVariant Identifiers: chr15:g.65321758G>A (hg19) chr15:g.65029420G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029420G>A , CM000677.2:g.65029420G>A GRCh38
NC_000015.9:g.65321758G>A , CM000677.1:g.65321758G>A GRCh37
NC_000015.8:g.63108811G>A NCBI36
NG_029184.1:g.5220C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.194C>T MANE Select ENSP00000220058.4:p.Ala65Val
ENST00000220058.8:c.194C>T ENSP00000220058.4:p.Ala65Val
ENST00000543678.1:c.194C>T ENSP00000443754.1:p.Ala65Val
ENST00000558460.5:c.194C>T ENSP00000452646.1:p.Ala65Val
ENST00000558614.1:n.155C>T
ENST00000559633.1:n.113C>T
ENST00000560717.5:c.179C>T ENSP00000457257.1:p.Ala60Val
NM_139242.3:c.194C>T NP_640335.2:p.Ala65Val
XM_005254158.5:c.194C>T XP_005254215.2:p.Ala65Val
XR_001751081.1:n.209C>T
NM_139242.4:c.194C>T MANE Select NP_640335.2:p.Ala65Val
Search 100 bp 5'
Search 100 bp 3'