Canonical Allele Identifier: CA645509394
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 438525
ClinVar RCV Id: RCV000505500

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22223856_22226500del , CM000685.2:g.22223856_22226500del GRCh38
NC_000023.10:g.22241973_22244617del , CM000685.1:g.22241973_22244617del GRCh37
NC_000023.9:g.22151894_22154538del NCBI36
NG_007563.2:g.196053_198697del

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.453+2113_511del (PHEX)
ENST00000683162.1:c.453+2113_511del (PHEX)
ENST00000683289.1:c.453+2113_511del (PHEX)
ENST00000683917.1:n.683+2113_741del (PHEX)
ENST00000684356.1:c.453+2113_511del (PHEX)
ENST00000684745.1:n.1573+2113_1631del (PHEX)
ENST00000379374.5:c.1899+2113_1957del (PHEX)
ENST00000379374.4:c.1899+2113_1957del (PHEX)
NM_000444.5:c.1899+2113_1957del (PHEX)
NM_001282754.1:c.1899+2113_1957del (PHEX)
XM_011545533.1:c.1143+2113_1201del (PHEX)
XM_011545534.1:c.1143+2113_1201del (PHEX)
XM_011545536.1:c.792+2113_850del (PHEX)
NR_073010.2:n.1048+970_1048+3614del (PTCHD1-AS)
XM_011545536.2:c.792+2113_850del (PHEX)
XM_017029579.1:c.1143+2113_1201del (PHEX)
XM_024452390.1:c.1608+2113_1666del (PHEX)
XR_001755695.1:n.2739+2113_2797del (PHEX)
NM_000444.6:c.1899+2113_1957del (PHEX)
NM_001282754.2:c.1899+2113_1957del (PHEX)