Canonical Allele Identifier: CA714892003

Gene: MTFMT

Linked Data

• dbSNP Id: rs1412912943
• gnomAD v3: 15-65029336-G-A
• gnomAD v4: 15-65029336-G-A
• MyVariant Identifiers: chr15:g.65321674G>A (hg19) ; chr15:g.65029336G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029336G>A , CM000677.2:g.65029336G>A	GRCh38
NC_000015.9:g.65321674G>A , CM000677.1:g.65321674G>A	GRCh37
NC_000015.8:g.63108727G>A	NCBI36
NG_029184.1:g.5304C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.209+69C>T MANE Select	ENSP00000220058.4:n.209+69C>T
ENST00000220058.8:c.209+69C>T	ENSP00000220058.4:n.209+69C>T
ENST00000543678.1:c.209+69C>T	ENSP00000443754.1:n.209+69C>T
ENST00000558460.5:c.209+69C>T	ENSP00000452646.1:n.209+69C>T
ENST00000558614.1:n.170+69C>T
ENST00000559633.1:n.128+69C>T
ENST00000560717.5:c.194+69C>T	ENSP00000457257.1:n.194+69C>T
NM_139242.3:c.209+69C>T	NP_640335.2:n.209+69C>T
XM_005254158.3:c.-131C>T	XP_005254215.1:n.-131C>T
XM_005254158.5:c.278C>T	XP_005254215.2:p.Pro93Leu
XR_001751081.1:n.293C>T
NM_139242.4:c.209+69C>T MANE Select	NP_640335.2:n.209+69C>T