Canonical Allele Identifier: CA413250097

Gene: PHF8

Linked Data

• ClinVar Variation Id: 441029
• ClinVar RCV Id: RCV000509211
• dbSNP Id: rs1557116325
• MyVariant Identifiers: chrX:g.54069221G>A (hg19) ; chrX:g.54042788G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54042788G>A , CM000685.2:g.54042788G>A	GRCh38
NC_000023.10:g.54069221G>A , CM000685.1:g.54069221G>A	GRCh37
NC_000023.9:g.54085946G>A	NCBI36
NG_021309.1:g.7349C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000686349.1:c.-60C>T	ENSP00000510424.1:n.-60C>T
ENST00000687764.1:c.-60C>T	ENSP00000509967.1:n.-60C>T
ENST00000338154.11:c.-60C>T MANE Select	ENSP00000338868.6:n.-60C>T
ENST00000322659.12:c.-60C>T	ENSP00000319473.8:n.-60C>T
ENST00000338154.10:c.-60C>T	ENSP00000338868.6:n.-60C>T
ENST00000338946.10:c.-60C>T	ENSP00000340051.6:n.-60C>T
ENST00000357988.9:c.49C>T	ENSP00000350676.5:p.Pro17Ser
ENST00000415025.5:c.-60C>T	ENSP00000404117.1:n.-60C>T
ENST00000425862.5:c.-60C>T	ENSP00000408113.1:n.-60C>T
ENST00000433120.5:c.-60C>T	ENSP00000410100.1:n.-60C>T
ENST00000437224.5:c.-60C>T	ENSP00000398995.1:n.-60C>T
ENST00000445025.1:c.-60C>T	ENSP00000416546.1:n.-60C>T
ENST00000453905.5:c.49C>T	ENSP00000405897.1:p.Pro17Ser
NM_001184896.1:c.49C>T	NP_001171825.1:p.Pro17Ser
NM_001184897.1:c.-60C>T	NP_001171826.1:n.-60C>T
NM_001184898.1:c.-60C>T	NP_001171827.1:n.-60C>T
NM_015107.2:c.-60C>T	NP_055922.1:n.-60C>T
XM_005261996.1:c.49C>T	XP_005262053.1:p.Pro17Ser
XM_005261997.2:c.-60C>T	XP_005262054.1:n.-60C>T
XM_005261999.1:c.-60C>T	XP_005262056.1:n.-60C>T
XM_005262000.1:c.49C>T	XP_005262057.1:p.Pro17Ser
XM_006724585.1:c.49C>T	XP_006724648.1:p.Pro17Ser
XM_011530778.1:c.49C>T	XP_011529080.1:p.Pro17Ser
XM_005261997.4:c.-60C>T	XP_005262054.1:n.-60C>T
XM_017029361.2:c.-60C>T	XP_016884850.1:n.-60C>T
XM_017029362.2:c.-60C>T	XP_016884851.1:n.-60C>T
NM_001184898.2:c.-60C>T	NP_001171827.1:n.-60C>T
NM_015107.3:c.-60C>T MANE Select	NP_055922.1:n.-60C>T
NM_001184897.2:c.-60C>T	NP_001171826.1:n.-60C>T