Canonical Allele Identifier: CA2430051090

Gene: PHF8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54042650G= , CM000685.2:g.54042650G=	GRCh38
NC_000023.10:g.54069083G= , CM000685.1:g.54069083G=	GRCh37
NC_000023.9:g.54085808G=	NCBI36
NG_021309.1:g.7487C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.79C=	ENSP00000340051.7:p.Gln27=
ENST00000396282.7:c.79C=	ENSP00000379578.3:p.Gln27=
ENST00000686349.1:c.79C=	ENSP00000510424.1:p.Gln27=
ENST00000687764.1:c.79C=	ENSP00000509967.1:p.Gln27=
ENST00000338154.11:c.79C= MANE Select	ENSP00000338868.6:p.Gln27=
ENST00000322659.12:c.79C=	ENSP00000319473.8:p.Gln27=
ENST00000338154.10:c.79C=	ENSP00000338868.6:p.Gln27=
ENST00000338946.10:c.79C=	ENSP00000340051.6:p.Gln27=
ENST00000357988.9:c.187C=	ENSP00000350676.5:p.Gln63=
ENST00000415025.5:c.79C=	ENSP00000404117.1:p.Gln27=
ENST00000425862.5:c.79C=	ENSP00000408113.1:p.Gln27=
ENST00000433120.5:c.79C=	ENSP00000410100.1:p.Gln27=
ENST00000437224.5:c.79C=	ENSP00000398995.1:p.Gln27=
ENST00000445025.1:c.79C=	ENSP00000416546.1:p.Gln27=
ENST00000453905.5:c.187C=	ENSP00000405897.1:p.Gln63=
ENST00000462182.1:n.67C=
NM_001184896.1:c.187C=	NP_001171825.1:p.Gln63=
NM_001184897.1:c.79C=	NP_001171826.1:p.Gln27=
NM_001184898.1:c.79C=	NP_001171827.1:p.Gln27=
NM_015107.2:c.79C=	NP_055922.1:p.Gln27=
XM_005261996.1:c.187C=	XP_005262053.1:p.Gln63=
XM_005261997.2:c.79C=	XP_005262054.1:p.Gln27=
XM_005261999.1:c.79C=	XP_005262056.1:p.Gln27=
XM_005262000.1:c.187C=	XP_005262057.1:p.Gln63=
XM_006724585.1:c.187C=	XP_006724648.1:p.Gln63=
XM_011530778.1:c.187C=	XP_011529080.1:p.Gln63=
XM_005261997.4:c.79C=	XP_005262054.1:p.Gln27=
XM_017029361.2:c.79C=	XP_016884850.1:p.Gln27=
XM_017029362.2:c.79C=	XP_016884851.1:p.Gln27=
NM_001184898.2:c.79C=	NP_001171827.1:p.Gln27=
NM_015107.3:c.79C= MANE Select	NP_055922.1:p.Gln27=
NM_001184897.2:c.79C=	NP_001171826.1:p.Gln27=