Canonical Allele Identifier: CA2580100485
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 2099810
ClinVar RCV Id: RCV003021903

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22247867_22247873delinsCTGGAA , CM000685.2:g.22247867_22247873delinsCTGGAA GRCh38
NC_000023.10:g.22265984_22265990delinsCTGGAA , CM000685.1:g.22265984_22265990delinsCTGGAA GRCh37
NC_000023.9:g.22175905_22175911delinsCTGGAA NCBI36
NG_007563.2:g.220064_220070delinsCTGGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000683162.1:c.*102_*108delinsCTGGAA (PHEX) ENSP00000508059.1:n.*102_*108delinsCTGGAA...
ENST00000683289.1:c.624+20256_624+20262delinsCTGGAA (PHEX) ENSP00000508195.1:n.624+20256_624+20262de...
ENST00000683917.1:n.948_954delinsCTGGAA (PHEX)
ENST00000684356.1:c.718_724delinsCTGGAA (PHEX) ENSP00000507619.1:p.Ser240LeufsTer18
ENST00000684745.1:n.1838_1844delinsCTGGAA (PHEX)
ENST00000379374.5:c.2164_2170delinsCTGGAA (PHEX) MANE Select ENSP00000368682.4:p.Ser722LeufsTer18
ENST00000379374.4:c.2164_2170delinsCTGGAA (PHEX) ENSP00000368682.4:p.Ser722LeufsTer18
NM_000444.5:c.2164_2170delinsCTGGAA (PHEX) NP_000435.3:p.Ser722LeufsTer18
NM_001282754.1:c.2087_*5delinsCTGGAA (PHEX) NP_001269683.1:n.[c.2087_*5delinsCTGGAA;T...
XM_011545533.1:c.1408_1414delinsCTGGAA (PHEX) XP_011543835.1:p.Ser470LeufsTer18
XM_011545534.1:c.1408_1414delinsCTGGAA (PHEX) XP_011543836.1:p.Ser470LeufsTer18
XM_011545536.1:c.1057_1063delinsCTGGAA (PHEX) XP_011543838.1:p.Ser353LeufsTer18
XR_950533.1:n.140+6066_140+6072delinsTTCCAG
XR_950534.1:n.127+6066_127+6072delinsTTCCAG
NR_073010.2:n.850+6066_850+6072delinsTTCCAG (PTCHD1-AS)
XM_011545536.2:c.1057_1063delinsCTGGAA (PHEX) XP_011543838.1:p.Ser353LeufsTer18
XM_017029579.1:c.1408_1414delinsCTGGAA (PHEX) XP_016885068.1:p.Ser470LeufsTer18
XM_024452390.1:c.1873_1879delinsCTGGAA (PHEX) XP_024308158.1:p.Ser625LeufsTer18
XR_001755695.1:n.3004_3010delinsCTGGAA (PHEX)
NM_000444.6:c.2164_2170delinsCTGGAA (PHEX) MANE Select NP_000435.3:p.Ser722LeufsTer18
NM_001282754.2:c.2087_*5delinsCTGGAA (PHEX) NP_001269683.1:n.[c.2087_*5delinsCTGGAA;T...