Canonical Allele Identifier: CA2430030611

Gene: PHF8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53984810_53984813delinsCCAG , CM000685.2:g.53984810_53984813delinsCCAG	GRCh38
NC_000023.10:g.54011243_54011246delinsCCAG , CM000685.1:g.54011243_54011246delinsCCAG	GRCh37
NC_000023.9:g.54027968_54027971delinsCCAG	NCBI36
NG_021309.1:g.65324_65327delinsCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.2140+101_2140+104delinsCTGG	ENSP00000340051.7:n.2140+101_2140+104delinsCTGG
ENST00000396282.7:c.2443+101_2443+104delinsCTGG	ENSP00000379578.3:n.2443+101_2443+104delinsCTGG
ENST00000686349.1:c.*898+101_*898+104delinsCTGG	ENSP00000510424.1:n.*898+101_*898+104delinsCTGG
ENST00000687764.1:c.*1885+101_*1885+104delinsCTGG	ENSP00000509967.1:n.*1885+101_*1885+104delinsCTGG
ENST00000691629.1:n.1807+101_1807+104delinsCTGG
ENST00000338154.11:c.2443+101_2443+104delinsCTGG MANE Select	ENSP00000338868.6:n.2443+101_2443+104delinsCTGG
ENST00000322659.12:c.2392+101_2392+104delinsCTGG	ENSP00000319473.8:n.2392+101_2392+104delinsCTGG
ENST00000338154.10:c.2443+101_2443+104delinsCTGG	ENSP00000338868.6:n.2443+101_2443+104delinsCTGG
ENST00000338946.10:c.2140+101_2140+104delinsCTGG	ENSP00000340051.6:n.2140+101_2140+104delinsCTGG
ENST00000357988.9:c.2551+101_2551+104delinsCTGG	ENSP00000350676.5:n.2551+101_2551+104delinsCTGG
ENST00000396282.6:c.2154+101_2154+104delinsCTGG
ENST00000443302.5:c.1733+101_1733+104delinsCTGG
ENST00000615775.4:c.870+101_870+104delinsCTGG	ENSP00000482159.1:n.870+101_870+104delinsCTGG
NM_001184896.1:c.2551+101_2551+104delinsCTGG	NP_001171825.1:n.2551+101_2551+104delinsCTGG
NM_001184897.1:c.2140+101_2140+104delinsCTGG	NP_001171826.1:n.2140+101_2140+104delinsCTGG
NM_001184898.1:c.2392+101_2392+104delinsCTGG	NP_001171827.1:n.2392+101_2392+104delinsCTGG
NM_015107.2:c.2443+101_2443+104delinsCTGG	NP_055922.1:n.2443+101_2443+104delinsCTGG
XM_005261996.1:c.2551+101_2551+104delinsCTGG	XP_005262053.1:n.2551+101_2551+104delinsCTGG
XM_005261997.2:c.2443+101_2443+104delinsCTGG	XP_005262054.1:n.2443+101_2443+104delinsCTGG
XM_005261999.1:c.2443+101_2443+104delinsCTGG	XP_005262056.1:n.2443+101_2443+104delinsCTGG
XM_005262000.1:c.2248+101_2248+104delinsCTGG	XP_005262057.1:n.2248+101_2248+104delinsCTGG
XM_006724585.1:c.2551+101_2551+104delinsCTGG	XP_006724648.1:n.2551+101_2551+104delinsCTGG
XM_011530778.1:c.2551+101_2551+104delinsCTGG	XP_011529080.1:n.2551+101_2551+104delinsCTGG
XM_005261997.4:c.2443+101_2443+104delinsCTGG	XP_005262054.1:n.2443+101_2443+104delinsCTGG
XM_017029361.2:c.2443+101_2443+104delinsCTGG	XP_016884850.1:n.2443+101_2443+104delinsCTGG
XM_017029362.2:c.2443+101_2443+104delinsCTGG	XP_016884851.1:n.2443+101_2443+104delinsCTGG
NM_001184898.2:c.2392+101_2392+104delinsCTGG	NP_001171827.1:n.2392+101_2392+104delinsCTGG
NM_015107.3:c.2443+101_2443+104delinsCTGG MANE Select	NP_055922.1:n.2443+101_2443+104delinsCTGG
NM_001184897.2:c.2140+101_2140+104delinsCTGG	NP_001171826.1:n.2140+101_2140+104delinsCTGG