Canonical Allele Identifier: CA915950786
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 803771
ClinVar RCV Id: RCV000990542
dbSNP Id: rs1602411514

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22226494_22226505dup , CM000685.2:g.22226494_22226505dup GRCh38
NC_000023.10:g.22244611_22244622dup , CM000685.1:g.22244611_22244622dup GRCh37
NC_000023.9:g.22154532_22154543dup NCBI36
NG_007563.2:g.198691_198702dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.505_*1dup (PHEX) ENSP00000508003.1:n.505_*1dup
ENST00000683162.1:c.505_516dup (PHEX) ENSP00000508059.1:p.Phe172_Arg173insArgGl...
ENST00000683289.1:c.505_516dup (PHEX) ENSP00000508195.1:p.Phe172_Arg173insArgGl...
ENST00000683917.1:n.735_746dup (PHEX)
ENST00000684356.1:c.505_516dup (PHEX) ENSP00000507619.1:p.Phe172_Arg173insArgGl...
ENST00000684745.1:n.1625_1636dup (PHEX)
ENST00000379374.5:c.1951_1962dup (PHEX) MANE Select ENSP00000368682.4:p.Phe654_Arg655insArgGl...
ENST00000379374.4:c.1951_1962dup (PHEX) ENSP00000368682.4:p.Phe654_Arg655insArgGl...
NM_000444.5:c.1951_1962dup (PHEX) NP_000435.3:p.Phe654_Arg655insArgGluAlaPh...
NM_001282754.1:c.1951_1962dup (PHEX) NP_001269683.1:p.Phe654_Arg655insArgGluAl...
XM_011545533.1:c.1195_1206dup (PHEX) XP_011543835.1:p.Phe402_Arg403insArgGluAl...
XM_011545534.1:c.1195_1206dup (PHEX) XP_011543836.1:p.Phe402_Arg403insArgGluAl...
XM_011545536.1:c.844_855dup (PHEX) XP_011543838.1:p.Phe285_Arg286insArgGluAl...
XR_950534.1:n.326-482_326-471dup
NR_073010.2:n.1048+965_1048+976dup (PTCHD1-AS)
XM_011545536.2:c.844_855dup (PHEX) XP_011543838.1:p.Phe285_Arg286insArgGluAl...
XM_017029579.1:c.1195_1206dup (PHEX) XP_016885068.1:p.Phe402_Arg403insArgGluAl...
XM_024452390.1:c.1660_1671dup (PHEX) XP_024308158.1:p.Phe557_Arg558insArgGluAl...
XR_001755695.1:n.2791_2802dup (PHEX)
NM_000444.6:c.1951_1962dup (PHEX) MANE Select NP_000435.3:p.Phe654_Arg655insArgGluAlaPh...
NM_001282754.2:c.1951_1962dup (PHEX) NP_001269683.1:p.Phe654_Arg655insArgGluAl...