Canonical Allele Identifier: CA2183422769

Gene: MTFMT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029296T= , CM000677.2:g.65029296T=	GRCh38
NC_000015.9:g.65321634T= , CM000677.1:g.65321634T=	GRCh37
NC_000015.8:g.63108687T=	NCBI36
NG_029184.1:g.5344A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.209+109A= MANE Select	ENSP00000220058.4:n.209+109A=
ENST00000220058.8:c.209+109A=	ENSP00000220058.4:n.209+109A=
ENST00000543678.1:c.209+109A=	ENSP00000443754.1:n.209+109A=
ENST00000558460.5:c.209+109A=	ENSP00000452646.1:n.209+109A=
ENST00000558614.1:n.170+109A=
ENST00000559633.1:n.128+109A=
ENST00000560717.5:c.194+109A=	ENSP00000457257.1:n.194+109A=
NM_139242.3:c.209+109A=	NP_640335.2:n.209+109A=
XM_005254158.3:c.-91A=	XP_005254215.1:n.-91A=
XM_005254158.5:c.318A=	XP_005254215.2:p.Ala106=
XR_001751081.1:n.333A=
NM_139242.4:c.209+109A= MANE Select	NP_640335.2:n.209+109A=