Canonical Allele Identifier: CA2693307160
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22221518_22221521dup , CM000685.2:g.22221518_22221521dup GRCh38
NC_000023.10:g.22239635_22239638dup , CM000685.1:g.22239635_22239638dup GRCh37
NC_000023.9:g.22149556_22149559dup NCBI36
NG_007563.2:g.193715_193718dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.323-95_323-92dup (PHEX) ENSP00000508003.1:n.323-95_323-92dup
ENST00000683162.1:c.323-95_323-92dup (PHEX) ENSP00000508059.1:n.323-95_323-92dup
ENST00000683289.1:c.323-95_323-92dup (PHEX) ENSP00000508195.1:n.323-95_323-92dup
ENST00000683917.1:n.553-95_553-92dup (PHEX)
ENST00000684356.1:c.323-95_323-92dup (PHEX) ENSP00000507619.1:n.323-95_323-92dup
ENST00000684745.1:n.1443-95_1443-92dup (PHEX)
ENST00000379374.5:c.1769-95_1769-92dup (PHEX) MANE Select ENSP00000368682.4:n.1769-95_1769-92dup
ENST00000379374.4:c.1769-95_1769-92dup (PHEX) ENSP00000368682.4:n.1769-95_1769-92dup
NM_000444.5:c.1769-95_1769-92dup (PHEX) NP_000435.3:n.1769-95_1769-92dup
NM_001282754.1:c.1769-95_1769-92dup (PHEX) NP_001269683.1:n.1769-95_1769-92dup
XM_011545533.1:c.1013-95_1013-92dup (PHEX) XP_011543835.1:n.1013-95_1013-92dup
XM_011545534.1:c.1013-95_1013-92dup (PHEX) XP_011543836.1:n.1013-95_1013-92dup
XM_011545536.1:c.662-95_662-92dup (PHEX) XP_011543838.1:n.662-95_662-92dup
NR_073010.2:n.1048+5951_1048+5954dup (PTCHD1-AS)
XM_011545536.2:c.662-95_662-92dup (PHEX) XP_011543838.1:n.662-95_662-92dup
XM_017029579.1:c.1013-95_1013-92dup (PHEX) XP_016885068.1:n.1013-95_1013-92dup
XM_024452390.1:c.1478-95_1478-92dup (PHEX) XP_024308158.1:n.1478-95_1478-92dup
XR_001755695.1:n.2609-95_2609-92dup (PHEX)
NM_000444.6:c.1769-95_1769-92dup (PHEX) MANE Select NP_000435.3:n.1769-95_1769-92dup
NM_001282754.2:c.1769-95_1769-92dup (PHEX) NP_001269683.1:n.1769-95_1769-92dup