Canonical Allele Identifier: CA657753401
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22221544G>A , CM000685.2:g.22221544G>A GRCh38
NC_000023.10:g.22239661G>A , CM000685.1:g.22239661G>A GRCh37
NC_000023.9:g.22149582G>A NCBI36
NG_007563.2:g.193741G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.323-69G>A (PHEX) ENSP00000508003.1:n.323-69G>A
ENST00000683162.1:c.323-69G>A (PHEX) ENSP00000508059.1:n.323-69G>A
ENST00000683289.1:c.323-69G>A (PHEX) ENSP00000508195.1:n.323-69G>A
ENST00000683917.1:n.553-69G>A (PHEX)
ENST00000684356.1:c.323-69G>A (PHEX) ENSP00000507619.1:n.323-69G>A
ENST00000684745.1:n.1443-69G>A (PHEX)
ENST00000379374.5:c.1769-69G>A (PHEX) MANE Select ENSP00000368682.4:n.1769-69G>A
ENST00000379374.4:c.1769-69G>A (PHEX) ENSP00000368682.4:n.1769-69G>A
NM_000444.5:c.1769-69G>A (PHEX) NP_000435.3:n.1769-69G>A
NM_001282754.1:c.1769-69G>A (PHEX) NP_001269683.1:n.1769-69G>A
XM_011545533.1:c.1013-69G>A (PHEX) XP_011543835.1:n.1013-69G>A
XM_011545534.1:c.1013-69G>A (PHEX) XP_011543836.1:n.1013-69G>A
XM_011545536.1:c.662-69G>A (PHEX) XP_011543838.1:n.662-69G>A
NR_073010.2:n.1048+5926C>T (PTCHD1-AS)
XM_011545536.2:c.662-69G>A (PHEX) XP_011543838.1:n.662-69G>A
XM_017029579.1:c.1013-69G>A (PHEX) XP_016885068.1:n.1013-69G>A
XM_024452390.1:c.1478-69G>A (PHEX) XP_024308158.1:n.1478-69G>A
XR_001755695.1:n.2609-69G>A (PHEX)
NM_000444.6:c.1769-69G>A (PHEX) MANE Select NP_000435.3:n.1769-69G>A
NM_001282754.2:c.1769-69G>A (PHEX) NP_001269683.1:n.1769-69G>A