Canonical Allele Identifier: CA490826929

Gene: MTFMT

Linked Data

• gnomAD v4: 15-65029437-G-T
• MyVariant Identifiers: chr15:g.65321775G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029437G>T , CM000677.2:g.65029437G>T	GRCh38
NC_000015.9:g.65321775G>T , CM000677.1:g.65321775G>T	GRCh37
NC_000015.8:g.63108828G>T	NCBI36
NG_029184.1:g.5203C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.177C>A MANE Select	ENSP00000220058.4:p.Ala59=
ENST00000220058.8:c.177C>A	ENSP00000220058.4:p.Ala59=
ENST00000543678.1:c.177C>A	ENSP00000443754.1:p.Ala59=
ENST00000558460.5:c.177C>A	ENSP00000452646.1:p.Ala59=
ENST00000558614.1:n.138C>A
ENST00000559633.1:n.96C>A
ENST00000560717.5:c.162C>A	ENSP00000457257.1:p.Ala54=
NM_139242.3:c.177C>A	NP_640335.2:p.Ala59=
XM_005254158.5:c.177C>A	XP_005254215.2:p.Ala59=
XR_001751081.1:n.192C>A
NM_139242.4:c.177C>A MANE Select	NP_640335.2:p.Ala59=