Canonical Allele Identifier: CA2580100529
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 2017104
ClinVar RCV Id: RCV002835035

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22227499_22227547dup , CM000685.2:g.22227499_22227547dup GRCh38
NC_000023.10:g.22245616_22245664dup , CM000685.1:g.22245616_22245664dup GRCh37
NC_000023.9:g.22155537_22155585dup NCBI36
NG_007563.2:g.199696_199744dup

Transcript Alleles

HGVS Amino-acid change
ENST00000683162.1:c.520-8_560dup (PHEX)
ENST00000683289.1:c.520-8_560dup (PHEX)
ENST00000683917.1:n.750-8_790dup (PHEX)
ENST00000684356.1:c.520-8_560dup (PHEX)
ENST00000684745.1:n.1640-8_1680dup (PHEX)
ENST00000379374.5:c.1966-8_2006dup (PHEX)
ENST00000379374.4:c.1966-8_2006dup (PHEX)
NM_000444.5:c.1966-8_2006dup (PHEX)
NM_001282754.1:c.1966-8_2006dup (PHEX)
XM_011545533.1:c.1210-8_1250dup (PHEX)
XM_011545534.1:c.1210-8_1250dup (PHEX)
XM_011545536.1:c.859-8_899dup (PHEX)
XR_950534.1:n.248_296dup
NR_073010.2:n.971_1019dup (PTCHD1-AS)
XM_011545536.2:c.859-8_899dup (PHEX)
XM_017029579.1:c.1210-8_1250dup (PHEX)
XM_024452390.1:c.1675-8_1715dup (PHEX)
XR_001755695.1:n.2806-8_2846dup (PHEX)
NM_000444.6:c.1966-8_2006dup (PHEX)
NM_001282754.2:c.1966-8_2006dup (PHEX)