Canonical Allele Identifier: CA533965

Gene: CFAP74

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1970722C>T , CM000663.2:g.1970722C>T	GRCh38
NC_000001.10:g.1902161C>T , CM000663.1:g.1902161C>T	GRCh37
NC_000001.9:g.1892021C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001304360.2:c.983G>A MANE Select	NP_001291289.1:p.Gly328Asp
ENST00000682832.2:c.983G>A MANE Select	ENSP00000508276.2:p.Gly328Asp
NM_001304360.1:c.983G>A	NP_001291289.1:p.Gly328Asp
ENST00000270720.11:n.1139G>A
ENST00000468610.5:n.1016G>A
ENST00000493964.5:c.983G>A	ENSP00000417061.2:p.Gly328Asp
XM_006710998.2:c.725G>A	XP_006711061.1:p.Gly242Asp
XM_011542331.1:c.983G>A	XP_011540633.1:p.Gly328Asp
XM_011542332.1:c.983G>A	XP_011540634.1:p.Gly328Asp
XM_011542333.1:c.740G>A	XP_011540635.1:p.Gly247Asp
XM_011542333.2:c.1052G>A	XP_011540635.2:p.Gly351Asp
XM_011542334.1:c.497G>A	XP_011540636.1:p.Gly166Asp
XM_011542335.1:c.476G>A	XP_011540637.1:p.Gly159Asp
XM_011542336.1:c.476G>A	XP_011540638.1:p.Gly159Asp
XM_011542336.3:c.476G>A	XP_011540638.1:p.Gly159Asp
XM_011542337.1:c.476G>A	XP_011540639.1:p.Gly159Asp
XM_017002641.1:c.1109G>A	XP_016858130.1:p.Gly370Asp
XM_017002642.1:c.1109G>A	XP_016858131.1:p.Gly370Asp
XM_017002643.1:c.1109G>A	XP_016858132.1:p.Gly370Asp