Canonical Allele Identifier: CA490826901

Gene: MTFMT

Linked Data

• MyVariant Identifiers: chr15:g.65321745G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029407G>C , CM000677.2:g.65029407G>C	GRCh38
NC_000015.9:g.65321745G>C , CM000677.1:g.65321745G>C	GRCh37
NC_000015.8:g.63108798G>C	NCBI36
NG_029184.1:g.5233C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.207C>G MANE Select	ENSP00000220058.4:p.Ala69=
ENST00000220058.8:c.207C>G	ENSP00000220058.4:p.Ala69=
ENST00000543678.1:c.207C>G	ENSP00000443754.1:p.Ala69=
ENST00000558460.5:c.207C>G	ENSP00000452646.1:p.Ala69=
ENST00000558614.1:n.168C>G
ENST00000559633.1:n.126C>G
ENST00000560717.5:c.192C>G	ENSP00000457257.1:p.Ala64=
NM_139242.3:c.207C>G	NP_640335.2:p.Ala69=
XM_005254158.5:c.207C>G	XP_005254215.2:p.Ala69=
XR_001751081.1:n.222C>G
NM_139242.4:c.207C>G MANE Select	NP_640335.2:p.Ala69=