Canonical Allele Identifier: CA10368413
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 1915378
ClinVar RCV Id: RCV002601438
dbSNP Id: rs767350363

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22227496_22227498del , CM000685.2:g.22227496_22227498del GRCh38
NC_000023.10:g.22245613_22245615del , CM000685.1:g.22245613_22245615del GRCh37
NC_000023.9:g.22155534_22155536del NCBI36
NG_007563.2:g.199693_199695del

Transcript Alleles

HGVS Amino-acid change
ENST00000683162.1:c.520-11_520-9del (PHEX) ENSP00000508059.1:n.520-11_520-9del
ENST00000683289.1:c.520-11_520-9del (PHEX) ENSP00000508195.1:n.520-11_520-9del
ENST00000683917.1:n.750-11_750-9del (PHEX)
ENST00000684356.1:c.520-11_520-9del (PHEX) ENSP00000507619.1:n.520-11_520-9del
ENST00000684745.1:n.1640-11_1640-9del (PHEX)
ENST00000379374.5:c.1966-11_1966-9del (PHEX) MANE Select ENSP00000368682.4:n.1966-11_1966-9del
ENST00000379374.4:c.1966-11_1966-9del (PHEX) ENSP00000368682.4:n.1966-11_1966-9del
NM_000444.5:c.1966-11_1966-9del (PHEX) NP_000435.3:n.1966-11_1966-9del
NM_001282754.1:c.1966-11_1966-9del (PHEX) NP_001269683.1:n.1966-11_1966-9del
XM_011545533.1:c.1210-11_1210-9del (PHEX) XP_011543835.1:n.1210-11_1210-9del
XM_011545534.1:c.1210-11_1210-9del (PHEX) XP_011543836.1:n.1210-11_1210-9del
XM_011545536.1:c.859-11_859-9del (PHEX) XP_011543838.1:n.859-11_859-9del
XR_950534.1:n.306_308del
NR_073010.2:n.1029_1031del (PTCHD1-AS)
XM_011545536.2:c.859-11_859-9del (PHEX) XP_011543838.1:n.859-11_859-9del
XM_017029579.1:c.1210-11_1210-9del (PHEX) XP_016885068.1:n.1210-11_1210-9del
XM_024452390.1:c.1675-11_1675-9del (PHEX) XP_024308158.1:n.1675-11_1675-9del
XR_001755695.1:n.2806-11_2806-9del (PHEX)
NM_000444.6:c.1966-11_1966-9del (PHEX) MANE Select NP_000435.3:n.1966-11_1966-9del
NM_001282754.2:c.1966-11_1966-9del (PHEX) NP_001269683.1:n.1966-11_1966-9del