Canonical Allele Identifier: CA392847000
Gene: MTFMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65006131T>A , CM000677.2:g.65006131T>A GRCh38
NC_000015.9:g.65298469T>A , CM000677.1:g.65298469T>A GRCh37
NC_000015.8:g.63085522T>A NCBI36
NG_029184.1:g.28509A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.874A>T MANE Select ENSP00000220058.4:p.Asn292Tyr
ENST00000220058.8:c.874A>T ENSP00000220058.4:p.Asn292Tyr
ENST00000558460.5:c.874A>T ENSP00000452646.1:p.Asn292Tyr
ENST00000560717.5:c.749A>T ENSP00000457257.1:n.749A>T
NM_139242.3:c.874A>T NP_640335.2:p.Asn292Tyr
XM_005254158.3:c.619A>T XP_005254215.1:p.Asn207Tyr
XM_005254158.5:c.1027A>T XP_005254215.2:p.Asn343Tyr
NM_139242.4:c.874A>T MANE Select NP_640335.2:p.Asn292Tyr