Canonical Allele Identifier: CA413251918

Gene: PHF8

Linked Data

• ClinVar Variation Id: 1790195
• ClinVar RCV Id: RCV002450129
• gnomAD v4: X-53984993-G-A
• MyVariant Identifiers: chrX:g.54011426G>A (hg19) ; chrX:g.53984993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53984993G>A , CM000685.2:g.53984993G>A	GRCh38
NC_000023.10:g.54011426G>A , CM000685.1:g.54011426G>A	GRCh37
NC_000023.9:g.54028151G>A	NCBI36
NG_021309.1:g.65144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.2061C>T	ENSP00000340051.7:p.Thr687=
ENST00000396282.7:c.2364C>T	ENSP00000379578.3:p.Thr788=
ENST00000686349.1:c.*819C>T	ENSP00000510424.1:n.*819C>T
ENST00000687764.1:c.*1806C>T	ENSP00000509967.1:n.*1806C>T
ENST00000691629.1:n.1728C>T
ENST00000338154.11:c.2364C>T MANE Select	ENSP00000338868.6:p.Thr788=
ENST00000322659.12:c.2313C>T	ENSP00000319473.8:p.Thr771=
ENST00000338154.10:c.2364C>T	ENSP00000338868.6:p.Thr788=
ENST00000338946.10:c.2061C>T	ENSP00000340051.6:p.Thr687=
ENST00000357988.9:c.2472C>T	ENSP00000350676.5:p.Thr824=
ENST00000396282.6:c.2075C>T
ENST00000443302.5:c.1654C>T
ENST00000615775.4:c.791C>T	ENSP00000482159.1:p.Pro264Leu
NM_001184896.1:c.2472C>T	NP_001171825.1:p.Thr824=
NM_001184897.1:c.2061C>T	NP_001171826.1:p.Thr687=
NM_001184898.1:c.2313C>T	NP_001171827.1:p.Thr771=
NM_015107.2:c.2364C>T	NP_055922.1:p.Thr788=
XM_005261996.1:c.2472C>T	XP_005262053.1:p.Thr824=
XM_005261997.2:c.2364C>T	XP_005262054.1:p.Thr788=
XM_005261999.1:c.2364C>T	XP_005262056.1:p.Thr788=
XM_005262000.1:c.2169C>T	XP_005262057.1:p.Thr723=
XM_006724585.1:c.2472C>T	XP_006724648.1:p.Thr824=
XM_011530778.1:c.2472C>T	XP_011529080.1:p.Thr824=
XM_005261997.4:c.2364C>T	XP_005262054.1:p.Thr788=
XM_017029361.2:c.2364C>T	XP_016884850.1:p.Thr788=
XM_017029362.2:c.2364C>T	XP_016884851.1:p.Thr788=
NM_001184898.2:c.2313C>T	NP_001171827.1:p.Thr771=
NM_015107.3:c.2364C>T MANE Select	NP_055922.1:p.Thr788=
NM_001184897.2:c.2061C>T	NP_001171826.1:p.Thr687=