Canonical Allele Identifier: CA2575758840
Gene: MTFMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029248G>C , CM000677.2:g.65029248G>C GRCh38
NC_000015.9:g.65321586G>C , CM000677.1:g.65321586G>C GRCh37
NC_000015.8:g.63108639G>C NCBI36
NG_029184.1:g.5392C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.209+157C>G MANE Select ENSP00000220058.4:n.209+157C>G
ENST00000220058.8:c.209+157C>G ENSP00000220058.4:n.209+157C>G
ENST00000543678.1:c.209+157C>G ENSP00000443754.1:n.209+157C>G
ENST00000558460.5:c.209+157C>G ENSP00000452646.1:n.209+157C>G
ENST00000558614.1:n.170+157C>G
ENST00000559633.1:n.128+157C>G
ENST00000560717.5:c.194+157C>G ENSP00000457257.1:n.194+157C>G
NM_139242.3:c.209+157C>G NP_640335.2:n.209+157C>G
XM_005254158.3:c.-47+4C>G XP_005254215.1:n.-47+4C>G
XM_005254158.5:c.362+4C>G XP_005254215.2:n.362+4C>G
XR_001751081.1:n.377+4C>G
NM_139242.4:c.209+157C>G MANE Select NP_640335.2:n.209+157C>G