Canonical Allele Identifier: CA2419220710

Gene: PHEX PTCHD1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247960C= , CM000685.2:g.22247960C=	GRCh38
NC_000023.10:g.22266077C= , CM000685.1:g.22266077C=	GRCh37
NC_000023.9:g.22175998C=	NCBI36
NG_007563.2:g.220157C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*195C= (PHEX)	ENSP00000508059.1:n.*195C=
ENST00000683289.1:c.624+20349C= (PHEX)	ENSP00000508195.1:n.624+20349C=
ENST00000683917.1:n.1041C= (PHEX)
ENST00000684356.1:c.*7C= (PHEX)	ENSP00000507619.1:n.*7C=
ENST00000684745.1:n.1931C= (PHEX)
ENST00000379374.5:c.*7C= (PHEX) MANE Select	ENSP00000368682.4:n.*7C=
ENST00000379374.4:c.*7C= (PHEX)	ENSP00000368682.4:n.*7C=
NM_000444.5:c.*7C= (PHEX)	NP_000435.3:n.*7C=
NM_001282754.1:c.*92C= (PHEX)	NP_001269683.1:n.*92C=
XM_011545533.1:c.*7C= (PHEX)	XP_011543835.1:n.*7C=
XM_011545534.1:c.*7C= (PHEX)	XP_011543836.1:n.*7C=
XM_011545536.1:c.*7C= (PHEX)	XP_011543838.1:n.*7C=
XR_950533.1:n.140+5979G=
XR_950534.1:n.127+5979G=
NR_073010.2:n.850+5979G= (PTCHD1-AS)
XM_011545536.2:c.*7C= (PHEX)	XP_011543838.1:n.*7C=
XM_017029579.1:c.*7C= (PHEX)	XP_016885068.1:n.*7C=
XM_024452390.1:c.*7C= (PHEX)	XP_024308158.1:n.*7C=
XR_001755695.1:n.3097C= (PHEX)
NM_000444.6:c.*7C= (PHEX) MANE Select	NP_000435.3:n.*7C=
NM_001282754.2:c.*92C= (PHEX)	NP_001269683.1:n.*92C=