Canonical Allele Identifier: CA2693307859
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22227464_22227470dup , CM000685.2:g.22227464_22227470dup GRCh38
NC_000023.10:g.22245581_22245587dup , CM000685.1:g.22245581_22245587dup GRCh37
NC_000023.9:g.22155502_22155508dup NCBI36
NG_007563.2:g.199661_199667dup

Transcript Alleles

HGVS Amino-acid change
ENST00000683162.1:c.520-43_520-37dup (PHEX) ENSP00000508059.1:n.520-43_520-37dup
ENST00000683289.1:c.520-43_520-37dup (PHEX) ENSP00000508195.1:n.520-43_520-37dup
ENST00000683917.1:n.750-43_750-37dup (PHEX)
ENST00000684356.1:c.520-43_520-37dup (PHEX) ENSP00000507619.1:n.520-43_520-37dup
ENST00000684745.1:n.1640-43_1640-37dup (PHEX)
ENST00000379374.5:c.1966-43_1966-37dup (PHEX) MANE Select ENSP00000368682.4:n.1966-43_1966-37dup
ENST00000379374.4:c.1966-43_1966-37dup (PHEX) ENSP00000368682.4:n.1966-43_1966-37dup
NM_000444.5:c.1966-43_1966-37dup (PHEX) NP_000435.3:n.1966-43_1966-37dup
NM_001282754.1:c.1966-43_1966-37dup (PHEX) NP_001269683.1:n.1966-43_1966-37dup
XM_011545533.1:c.1210-43_1210-37dup (PHEX) XP_011543835.1:n.1210-43_1210-37dup
XM_011545534.1:c.1210-43_1210-37dup (PHEX) XP_011543836.1:n.1210-43_1210-37dup
XM_011545536.1:c.859-43_859-37dup (PHEX) XP_011543838.1:n.859-43_859-37dup
XR_950534.1:n.325_325+6dup
NR_073010.2:n.1048_1048+6dup (PTCHD1-AS)
XM_011545536.2:c.859-43_859-37dup (PHEX) XP_011543838.1:n.859-43_859-37dup
XM_017029579.1:c.1210-43_1210-37dup (PHEX) XP_016885068.1:n.1210-43_1210-37dup
XM_024452390.1:c.1675-43_1675-37dup (PHEX) XP_024308158.1:n.1675-43_1675-37dup
XR_001755695.1:n.2806-43_2806-37dup (PHEX)
NM_000444.6:c.1966-43_1966-37dup (PHEX) MANE Select NP_000435.3:n.1966-43_1966-37dup
NM_001282754.2:c.1966-43_1966-37dup (PHEX) NP_001269683.1:n.1966-43_1966-37dup