Canonical Allele Identifier: CA490827007

Gene: MTFMT

Linked Data

• MyVariant Identifiers: chr15:g.65321886C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029548C>G , CM000677.2:g.65029548C>G	GRCh38
NC_000015.9:g.65321886C>G , CM000677.1:g.65321886C>G	GRCh37
NC_000015.8:g.63108939C>G	NCBI36
NG_029184.1:g.5092G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.66G>C MANE Select	ENSP00000220058.4:p.Pro22=
ENST00000220058.8:c.66G>C	ENSP00000220058.4:p.Pro22=
ENST00000543678.1:c.66G>C	ENSP00000443754.1:p.Pro22=
ENST00000558460.5:c.66G>C	ENSP00000452646.1:p.Pro22=
ENST00000558614.1:n.27G>C
ENST00000560717.5:c.51G>C	ENSP00000457257.1:p.Pro17=
NM_139242.3:c.66G>C	NP_640335.2:p.Pro22=
XM_005254158.5:c.66G>C	XP_005254215.2:p.Pro22=
XR_001751081.1:n.81G>C
NM_139242.4:c.66G>C MANE Select	NP_640335.2:p.Pro22=