Canonical Allele Identifier: CA413251816

Gene: PHF8

Linked Data

• MyVariant Identifiers: chrX:g.54011411C>A (hg19) ; chrX:g.53984978C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53984978C>A , CM000685.2:g.53984978C>A	GRCh38
NC_000023.10:g.54011411C>A , CM000685.1:g.54011411C>A	GRCh37
NC_000023.9:g.54028136C>A	NCBI36
NG_021309.1:g.65159G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.2076G>T	ENSP00000340051.7:p.Glu692Asp
ENST00000396282.7:c.2379G>T	ENSP00000379578.3:p.Glu793Asp
ENST00000686349.1:c.*834G>T	ENSP00000510424.1:n.*834G>T
ENST00000687764.1:c.*1821G>T	ENSP00000509967.1:n.*1821G>T
ENST00000691629.1:n.1743G>T
ENST00000338154.11:c.2379G>T MANE Select	ENSP00000338868.6:p.Glu793Asp
ENST00000322659.12:c.2328G>T	ENSP00000319473.8:p.Glu776Asp
ENST00000338154.10:c.2379G>T	ENSP00000338868.6:p.Glu793Asp
ENST00000338946.10:c.2076G>T	ENSP00000340051.6:p.Glu692Asp
ENST00000357988.9:c.2487G>T	ENSP00000350676.5:p.Glu829Asp
ENST00000396282.6:c.2090G>T
ENST00000443302.5:c.1669G>T
ENST00000615775.4:c.806G>T	ENSP00000482159.1:p.Arg269Met
NM_001184896.1:c.2487G>T	NP_001171825.1:p.Glu829Asp
NM_001184897.1:c.2076G>T	NP_001171826.1:p.Glu692Asp
NM_001184898.1:c.2328G>T	NP_001171827.1:p.Glu776Asp
NM_015107.2:c.2379G>T	NP_055922.1:p.Glu793Asp
XM_005261996.1:c.2487G>T	XP_005262053.1:p.Glu829Asp
XM_005261997.2:c.2379G>T	XP_005262054.1:p.Glu793Asp
XM_005261999.1:c.2379G>T	XP_005262056.1:p.Glu793Asp
XM_005262000.1:c.2184G>T	XP_005262057.1:p.Glu728Asp
XM_006724585.1:c.2487G>T	XP_006724648.1:p.Glu829Asp
XM_011530778.1:c.2487G>T	XP_011529080.1:p.Glu829Asp
XM_005261997.4:c.2379G>T	XP_005262054.1:p.Glu793Asp
XM_017029361.2:c.2379G>T	XP_016884850.1:p.Glu793Asp
XM_017029362.2:c.2379G>T	XP_016884851.1:p.Glu793Asp
NM_001184898.2:c.2328G>T	NP_001171827.1:p.Glu776Asp
NM_015107.3:c.2379G>T MANE Select	NP_055922.1:p.Glu793Asp
NM_001184897.2:c.2076G>T	NP_001171826.1:p.Glu692Asp