Canonical Allele Identifier: CA413252727

Gene: PHF8

Linked Data

• MyVariant Identifiers: chrX:g.54011543C>A (hg19) ; chrX:g.53985110C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53985110C>A , CM000685.2:g.53985110C>A	GRCh38
NC_000023.10:g.54011543C>A , CM000685.1:g.54011543C>A	GRCh37
NC_000023.9:g.54028268C>A	NCBI36
NG_021309.1:g.65027G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338946.11:c.1944G>T	ENSP00000340051.7:p.Gly648=
ENST00000396282.7:c.2247G>T	ENSP00000379578.3:p.Gly749=
ENST00000686349.1:c.*702G>T	ENSP00000510424.1:n.*702G>T
ENST00000687764.1:c.*1689G>T	ENSP00000509967.1:n.*1689G>T
ENST00000691629.1:n.1611G>T
ENST00000338154.11:c.2247G>T MANE Select	ENSP00000338868.6:p.Gly749=
ENST00000322659.12:c.2196G>T	ENSP00000319473.8:p.Gly732=
ENST00000338154.10:c.2247G>T	ENSP00000338868.6:p.Gly749=
ENST00000338946.10:c.1944G>T	ENSP00000340051.6:p.Gly648=
ENST00000357988.9:c.2355G>T	ENSP00000350676.5:p.Gly785=
ENST00000396282.6:c.1958G>T
ENST00000443302.5:c.1537G>T
ENST00000615775.4:c.674G>T	ENSP00000482159.1:p.Gly225Val
NM_001184896.1:c.2355G>T	NP_001171825.1:p.Gly785=
NM_001184897.1:c.1944G>T	NP_001171826.1:p.Gly648=
NM_001184898.1:c.2196G>T	NP_001171827.1:p.Gly732=
NM_015107.2:c.2247G>T	NP_055922.1:p.Gly749=
XM_005261996.1:c.2355G>T	XP_005262053.1:p.Gly785=
XM_005261997.2:c.2247G>T	XP_005262054.1:p.Gly749=
XM_005261999.1:c.2247G>T	XP_005262056.1:p.Gly749=
XM_005262000.1:c.2052G>T	XP_005262057.1:p.Gly684=
XM_006724585.1:c.2355G>T	XP_006724648.1:p.Gly785=
XM_011530778.1:c.2355G>T	XP_011529080.1:p.Gly785=
XM_005261997.4:c.2247G>T	XP_005262054.1:p.Gly749=
XM_017029361.2:c.2247G>T	XP_016884850.1:p.Gly749=
XM_017029362.2:c.2247G>T	XP_016884851.1:p.Gly749=
NM_001184898.2:c.2196G>T	NP_001171827.1:p.Gly732=
NM_015107.3:c.2247G>T MANE Select	NP_055922.1:p.Gly749=
NM_001184897.2:c.1944G>T	NP_001171826.1:p.Gly648=