Canonical Allele Identifier: CA392863117

Gene: MTFMT

Linked Data

• MyVariant Identifiers: chr15:g.65321866A>C (hg19) ; chr15:g.65029528A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029528A>C , CM000677.2:g.65029528A>C	GRCh38
NC_000015.9:g.65321866A>C , CM000677.1:g.65321866A>C	GRCh37
NC_000015.8:g.63108919A>C	NCBI36
NG_029184.1:g.5112T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.86T>G MANE Select	ENSP00000220058.4:p.Leu29Arg
ENST00000220058.8:c.86T>G	ENSP00000220058.4:p.Leu29Arg
ENST00000543678.1:c.86T>G	ENSP00000443754.1:p.Leu29Arg
ENST00000558460.5:c.86T>G	ENSP00000452646.1:p.Leu29Arg
ENST00000558614.1:n.47T>G
ENST00000559633.1:n.5T>G
ENST00000560717.5:c.71T>G	ENSP00000457257.1:p.Leu24Arg
NM_139242.3:c.86T>G	NP_640335.2:p.Leu29Arg
XM_005254158.5:c.86T>G	XP_005254215.2:p.Leu29Arg
XR_001751081.1:n.101T>G
NM_139242.4:c.86T>G MANE Select	NP_640335.2:p.Leu29Arg