Canonical Allele Identifier: CA392862819

Gene: MTFMT

Linked Data

• MyVariant Identifiers: chr15:g.65321834A>T (hg19) ; chr15:g.65029496A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029496A>T , CM000677.2:g.65029496A>T	GRCh38
NC_000015.9:g.65321834A>T , CM000677.1:g.65321834A>T	GRCh37
NC_000015.8:g.63108887A>T	NCBI36
NG_029184.1:g.5144T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.118T>A MANE Select	ENSP00000220058.4:p.Ser40Thr
ENST00000220058.8:c.118T>A	ENSP00000220058.4:p.Ser40Thr
ENST00000543678.1:c.118T>A	ENSP00000443754.1:p.Ser40Thr
ENST00000558460.5:c.118T>A	ENSP00000452646.1:p.Ser40Thr
ENST00000558614.1:n.79T>A
ENST00000559633.1:n.37T>A
ENST00000560717.5:c.103T>A	ENSP00000457257.1:p.Ser35Thr
NM_139242.3:c.118T>A	NP_640335.2:p.Ser40Thr
XM_005254158.5:c.118T>A	XP_005254215.2:p.Ser40Thr
XR_001751081.1:n.133T>A
NM_139242.4:c.118T>A MANE Select	NP_640335.2:p.Ser40Thr