Canonical Allele Identifier: CA412575548

Gene: PHEX PTCHD1-AS

Linked Data

• ClinVar Variation Id: 803778
• ClinVar RCV Id: RCV000990549 ; RCV003679024
• dbSNP Id: rs1602442819
• MyVariant Identifiers: chrX:g.22266056T>C (hg19) ; chrX:g.22247939T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247939T>C , CM000685.2:g.22247939T>C	GRCh38
NC_000023.10:g.22266056T>C , CM000685.1:g.22266056T>C	GRCh37
NC_000023.9:g.22175977T>C	NCBI36
NG_007563.2:g.220136T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*174T>C (PHEX)	ENSP00000508059.1:n.*174T>C
ENST00000683289.1:c.624+20328T>C (PHEX)	ENSP00000508195.1:n.624+20328T>C
ENST00000683917.1:n.1020T>C (PHEX)
ENST00000684356.1:c.790T>C (PHEX)	ENSP00000507619.1:p.Cys264Arg
ENST00000684745.1:n.1910T>C (PHEX)
ENST00000379374.5:c.2236T>C (PHEX) MANE Select	ENSP00000368682.4:p.Cys746Arg
ENST00000379374.4:c.2236T>C (PHEX)	ENSP00000368682.4:p.Cys746Arg
NM_000444.5:c.2236T>C (PHEX)	NP_000435.3:p.Cys746Arg
NM_001282754.1:c.*71T>C (PHEX)	NP_001269683.1:n.*71T>C
XM_011545533.1:c.1480T>C (PHEX)	XP_011543835.1:p.Cys494Arg
XM_011545534.1:c.1480T>C (PHEX)	XP_011543836.1:p.Cys494Arg
XM_011545536.1:c.1129T>C (PHEX)	XP_011543838.1:p.Cys377Arg
XR_950533.1:n.140+6000A>G
XR_950534.1:n.127+6000A>G
NR_073010.2:n.850+6000A>G (PTCHD1-AS)
XM_011545536.2:c.1129T>C (PHEX)	XP_011543838.1:p.Cys377Arg
XM_017029579.1:c.1480T>C (PHEX)	XP_016885068.1:p.Cys494Arg
XM_024452390.1:c.1945T>C (PHEX)	XP_024308158.1:p.Cys649Arg
XR_001755695.1:n.3076T>C (PHEX)
NM_000444.6:c.2236T>C (PHEX) MANE Select	NP_000435.3:p.Cys746Arg
NM_001282754.2:c.*71T>C (PHEX)	NP_001269683.1:n.*71T>C