Canonical Allele Identifier: CA2183422752

Gene: MTFMT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029266A= , CM000677.2:g.65029266A=	GRCh38
NC_000015.9:g.65321604A= , CM000677.1:g.65321604A=	GRCh37
NC_000015.8:g.63108657A=	NCBI36
NG_029184.1:g.5374T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.209+139T= MANE Select	ENSP00000220058.4:n.209+139T=
ENST00000220058.8:c.209+139T=	ENSP00000220058.4:n.209+139T=
ENST00000543678.1:c.209+139T=	ENSP00000443754.1:n.209+139T=
ENST00000558460.5:c.209+139T=	ENSP00000452646.1:n.209+139T=
ENST00000558614.1:n.170+139T=
ENST00000559633.1:n.128+139T=
ENST00000560717.5:c.194+139T=	ENSP00000457257.1:n.194+139T=
NM_139242.3:c.209+139T=	NP_640335.2:n.209+139T=
XM_005254158.3:c.-61T=	XP_005254215.1:n.-61T=
XM_005254158.5:c.348T=	XP_005254215.2:p.Leu116=
XR_001751081.1:n.363T=
NM_139242.4:c.209+139T= MANE Select	NP_640335.2:n.209+139T=