Canonical Allele Identifier: CA392863265
Gene: MTFMT HGNC NCBI

Linked Data

dbSNP Id: rs928783546

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029546C>T , CM000677.2:g.65029546C>T GRCh38
NC_000015.9:g.65321884C>T , CM000677.1:g.65321884C>T GRCh37
NC_000015.8:g.63108937C>T NCBI36
NG_029184.1:g.5094G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.68G>A MANE Select ENSP00000220058.4:p.Ser23Asn
ENST00000220058.8:c.68G>A ENSP00000220058.4:p.Ser23Asn
ENST00000543678.1:c.68G>A ENSP00000443754.1:p.Ser23Asn
ENST00000558460.5:c.68G>A ENSP00000452646.1:p.Ser23Asn
ENST00000558614.1:n.29G>A
ENST00000560717.5:c.53G>A ENSP00000457257.1:p.Ser18Asn
NM_139242.3:c.68G>A NP_640335.2:p.Ser23Asn
XM_005254158.5:c.68G>A XP_005254215.2:p.Ser23Asn
XR_001751081.1:n.83G>A
NM_139242.4:c.68G>A MANE Select NP_640335.2:p.Ser23Asn