Canonical Allele Identifier: CA413250499

Gene: PHF8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54044882C>A , CM000685.2:g.54044882C>A	GRCh38
NC_000023.10:g.54071315C>A , CM000685.1:g.54071315C>A	GRCh37
NC_000023.9:g.54088040C>A	NCBI36
NG_021309.1:g.5255G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357988.9:c.9G>T	ENSP00000350676.5:p.Arg3Ser
ENST00000437224.5:c.-89G>T	ENSP00000398995.1:n.-89G>T
ENST00000453905.5:c.9G>T	ENSP00000405897.1:p.Arg3Ser
NM_001184896.1:c.9G>T	NP_001171825.1:p.Arg3Ser
XM_005261996.1:c.9G>T	XP_005262053.1:p.Arg3Ser
XM_005262000.1:c.9G>T	XP_005262057.1:p.Arg3Ser
XM_006724585.1:c.9G>T	XP_006724648.1:p.Arg3Ser
XM_011530778.1:c.9G>T	XP_011529080.1:p.Arg3Ser