Canonical Allele Identifier: CA2430030646

Gene: PHF8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53984915A= , CM000685.2:g.53984915A=	GRCh38
NC_000023.10:g.54011348A= , CM000685.1:g.54011348A=	GRCh37
NC_000023.9:g.54028073A=	NCBI36
NG_021309.1:g.65222T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.2139T=	ENSP00000340051.7:p.Tyr713=
ENST00000396282.7:c.2442T=	ENSP00000379578.3:p.Tyr814=
ENST00000686349.1:c.*897T=	ENSP00000510424.1:n.*897T=
ENST00000687764.1:c.*1884T=	ENSP00000509967.1:n.*1884T=
ENST00000691629.1:n.1806T=
ENST00000338154.11:c.2442T= MANE Select	ENSP00000338868.6:p.Tyr814=
ENST00000322659.12:c.2391T=	ENSP00000319473.8:p.Tyr797=
ENST00000338154.10:c.2442T=	ENSP00000338868.6:p.Tyr814=
ENST00000338946.10:c.2139T=	ENSP00000340051.6:p.Tyr713=
ENST00000357988.9:c.2550T=	ENSP00000350676.5:p.Tyr850=
ENST00000396282.6:c.2153T=
ENST00000443302.5:c.1732T=
ENST00000615775.4:c.869T=	ENSP00000482159.1:p.Ile290=
NM_001184896.1:c.2550T=	NP_001171825.1:p.Tyr850=
NM_001184897.1:c.2139T=	NP_001171826.1:p.Tyr713=
NM_001184898.1:c.2391T=	NP_001171827.1:p.Tyr797=
NM_015107.2:c.2442T=	NP_055922.1:p.Tyr814=
XM_005261996.1:c.2550T=	XP_005262053.1:p.Tyr850=
XM_005261997.2:c.2442T=	XP_005262054.1:p.Tyr814=
XM_005261999.1:c.2442T=	XP_005262056.1:p.Tyr814=
XM_005262000.1:c.2247T=	XP_005262057.1:p.Tyr749=
XM_006724585.1:c.2550T=	XP_006724648.1:p.Tyr850=
XM_011530778.1:c.2550T=	XP_011529080.1:p.Tyr850=
XM_005261997.4:c.2442T=	XP_005262054.1:p.Tyr814=
XM_017029361.2:c.2442T=	XP_016884850.1:p.Tyr814=
XM_017029362.2:c.2442T=	XP_016884851.1:p.Tyr814=
NM_001184898.2:c.2391T=	NP_001171827.1:p.Tyr797=
NM_015107.3:c.2442T= MANE Select	NP_055922.1:p.Tyr814=
NM_001184897.2:c.2139T=	NP_001171826.1:p.Tyr713=