Canonical Allele Identifier: CA2430030768

Gene: PHF8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53985316T= , CM000685.2:g.53985316T=	GRCh38
NC_000023.10:g.54011749T= , CM000685.1:g.54011749T=	GRCh37
NC_000023.9:g.54028474T=	NCBI36
NG_021309.1:g.64821A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.1827-89A=	ENSP00000340051.7:n.1827-89A=
ENST00000396282.7:c.2130-89A=	ENSP00000379578.3:n.2130-89A=
ENST00000686349.1:c.*496A=	ENSP00000510424.1:n.*496A=
ENST00000687764.1:c.*1483A=	ENSP00000509967.1:n.*1483A=
ENST00000691629.1:n.1494-89A=
ENST00000338154.11:c.2130-89A= MANE Select	ENSP00000338868.6:n.2130-89A=
ENST00000322659.12:c.2079-89A=	ENSP00000319473.8:n.2079-89A=
ENST00000338154.10:c.2130-89A=	ENSP00000338868.6:n.2130-89A=
ENST00000338946.10:c.1827-89A=	ENSP00000340051.6:n.1827-89A=
ENST00000357988.9:c.2238-89A=	ENSP00000350676.5:n.2238-89A=
ENST00000396282.6:c.1841-89A=
ENST00000443302.5:c.1420-89A=
ENST00000615775.4:c.557-89A=	ENSP00000482159.1:n.557-89A=
NM_001184896.1:c.2238-89A=	NP_001171825.1:n.2238-89A=
NM_001184897.1:c.1827-89A=	NP_001171826.1:n.1827-89A=
NM_001184898.1:c.2079-89A=	NP_001171827.1:n.2079-89A=
NM_015107.2:c.2130-89A=	NP_055922.1:n.2130-89A=
XM_005261996.1:c.2238-89A=	XP_005262053.1:n.2238-89A=
XM_005261997.2:c.2130-89A=	XP_005262054.1:n.2130-89A=
XM_005261999.1:c.2130-89A=	XP_005262056.1:n.2130-89A=
XM_005262000.1:c.1935-89A=	XP_005262057.1:n.1935-89A=
XM_006724585.1:c.2238-89A=	XP_006724648.1:n.2238-89A=
XM_011530778.1:c.2238-89A=	XP_011529080.1:n.2238-89A=
XM_005261997.4:c.2130-89A=	XP_005262054.1:n.2130-89A=
XM_017029361.2:c.2130-89A=	XP_016884850.1:n.2130-89A=
XM_017029362.2:c.2130-89A=	XP_016884851.1:n.2130-89A=
NM_001184898.2:c.2079-89A=	NP_001171827.1:n.2079-89A=
NM_015107.3:c.2130-89A= MANE Select	NP_055922.1:n.2130-89A=
NM_001184897.2:c.1827-89A=	NP_001171826.1:n.1827-89A=