Canonical Allele Identifier: CA16609167

Gene: PHEX PTCHD1-AS

Linked Data

• ClinVar Variation Id: 392729
• ClinVar RCV Id: RCV000419875
• dbSNP Id: rs1057524608
• MyVariant Identifiers: chrX:g.22237225G>T (hg19) ; chrX:g.22219108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22219108G>T , CM000685.2:g.22219108G>T	GRCh38
NC_000023.10:g.22237225G>T , CM000685.1:g.22237225G>T	GRCh37
NC_000023.9:g.22147146G>T	NCBI36
NG_007563.2:g.191305G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682888.1:c.322+5G>T (PHEX)	ENSP00000508003.1:n.322+5G>T
ENST00000683162.1:c.322+5G>T (PHEX)	ENSP00000508059.1:n.322+5G>T
ENST00000683289.1:c.322+5G>T (PHEX)	ENSP00000508195.1:n.322+5G>T
ENST00000683917.1:n.552+5G>T (PHEX)
ENST00000684356.1:c.322+5G>T (PHEX)	ENSP00000507619.1:n.322+5G>T
ENST00000684745.1:n.1442+5G>T (PHEX)
ENST00000379374.5:c.1768+5G>T (PHEX) MANE Select	ENSP00000368682.4:n.1768+5G>T
ENST00000379374.4:c.1768+5G>T (PHEX)	ENSP00000368682.4:n.1768+5G>T
NM_000444.5:c.1768+5G>T (PHEX)	NP_000435.3:n.1768+5G>T
NM_001282754.1:c.1768+5G>T (PHEX)	NP_001269683.1:n.1768+5G>T
XM_011545533.1:c.1012+5G>T (PHEX)	XP_011543835.1:n.1012+5G>T
XM_011545534.1:c.1012+5G>T (PHEX)	XP_011543836.1:n.1012+5G>T
XM_011545536.1:c.661+5G>T (PHEX)	XP_011543838.1:n.661+5G>T
NR_073010.2:n.1048+8362C>A (PTCHD1-AS)
XM_011545536.2:c.661+5G>T (PHEX)	XP_011543838.1:n.661+5G>T
XM_017029579.1:c.1012+5G>T (PHEX)	XP_016885068.1:n.1012+5G>T
XM_024452390.1:c.1477+5G>T (PHEX)	XP_024308158.1:n.1477+5G>T
XR_001755695.1:n.2608+5G>T (PHEX)
NM_000444.6:c.1768+5G>T (PHEX) MANE Select	NP_000435.3:n.1768+5G>T
NM_001282754.2:c.1768+5G>T (PHEX)	NP_001269683.1:n.1768+5G>T