Canonical Allele Identifier: CA490826924
Gene: MTFMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65321772G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029434G>A , CM000677.2:g.65029434G>A GRCh38
NC_000015.9:g.65321772G>A , CM000677.1:g.65321772G>A GRCh37
NC_000015.8:g.63108825G>A NCBI36
NG_029184.1:g.5206C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.180C>T MANE Select ENSP00000220058.4:p.Arg60=
ENST00000220058.8:c.180C>T ENSP00000220058.4:p.Arg60=
ENST00000543678.1:c.180C>T ENSP00000443754.1:p.Arg60=
ENST00000558460.5:c.180C>T ENSP00000452646.1:p.Arg60=
ENST00000558614.1:n.141C>T
ENST00000559633.1:n.99C>T
ENST00000560717.5:c.165C>T ENSP00000457257.1:p.Arg55=
NM_139242.3:c.180C>T NP_640335.2:p.Arg60=
XM_005254158.5:c.180C>T XP_005254215.2:p.Arg60=
XR_001751081.1:n.195C>T
NM_139242.4:c.180C>T MANE Select NP_640335.2:p.Arg60=