Canonical Allele Identifier: CA2419209583
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22221646C= , CM000685.2:g.22221646C= GRCh38
NC_000023.10:g.22239763C= , CM000685.1:g.22239763C= GRCh37
NC_000023.9:g.22149684C= NCBI36
NG_007563.2:g.193843C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.356C= (PHEX) ENSP00000508003.1:p.Pro119=
ENST00000683162.1:c.356C= (PHEX) ENSP00000508059.1:p.Pro119=
ENST00000683289.1:c.356C= (PHEX) ENSP00000508195.1:p.Pro119=
ENST00000683917.1:n.586C= (PHEX)
ENST00000684356.1:c.356C= (PHEX) ENSP00000507619.1:p.Pro119=
ENST00000684745.1:n.1476C= (PHEX)
ENST00000379374.5:c.1802C= (PHEX) MANE Select ENSP00000368682.4:p.Pro601=
ENST00000379374.4:c.1802C= (PHEX) ENSP00000368682.4:p.Pro601=
NM_000444.5:c.1802C= (PHEX) NP_000435.3:p.Pro601=
NM_001282754.1:c.1802C= (PHEX) NP_001269683.1:p.Pro601=
XM_011545533.1:c.1046C= (PHEX) XP_011543835.1:p.Pro349=
XM_011545534.1:c.1046C= (PHEX) XP_011543836.1:p.Pro349=
XM_011545536.1:c.695C= (PHEX) XP_011543838.1:p.Pro232=
NR_073010.2:n.1048+5824G= (PTCHD1-AS)
XM_011545536.2:c.695C= (PHEX) XP_011543838.1:p.Pro232=
XM_017029579.1:c.1046C= (PHEX) XP_016885068.1:p.Pro349=
XM_024452390.1:c.1511C= (PHEX) XP_024308158.1:p.Pro504=
XR_001755695.1:n.2642C= (PHEX)
NM_000444.6:c.1802C= (PHEX) MANE Select NP_000435.3:p.Pro601=
NM_001282754.2:c.1802C= (PHEX) NP_001269683.1:p.Pro601=