Canonical Allele Identifier: CA2419208629

Gene: PHEX PTCHD1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22218827C= , CM000685.2:g.22218827C=	GRCh38
NC_000023.10:g.22236944C= , CM000685.1:g.22236944C=	GRCh37
NC_000023.9:g.22146865C=	NCBI36
NG_007563.2:g.191024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.255-209C= (PHEX)	ENSP00000508003.1:n.255-209C=
ENST00000683162.1:c.255-209C= (PHEX)	ENSP00000508059.1:n.255-209C=
ENST00000683289.1:c.255-209C= (PHEX)	ENSP00000508195.1:n.255-209C=
ENST00000683917.1:n.485-209C= (PHEX)
ENST00000684356.1:c.255-209C= (PHEX)	ENSP00000507619.1:n.255-209C=
ENST00000684745.1:n.1375-209C= (PHEX)
ENST00000379374.5:c.1701-209C= (PHEX) MANE Select	ENSP00000368682.4:n.1701-209C=
ENST00000379374.4:c.1701-209C= (PHEX)	ENSP00000368682.4:n.1701-209C=
NM_000444.5:c.1701-209C= (PHEX)	NP_000435.3:n.1701-209C=
NM_001282754.1:c.1701-209C= (PHEX)	NP_001269683.1:n.1701-209C=
XM_011545533.1:c.945-209C= (PHEX)	XP_011543835.1:n.945-209C=
XM_011545534.1:c.945-209C= (PHEX)	XP_011543836.1:n.945-209C=
XM_011545536.1:c.594-209C= (PHEX)	XP_011543838.1:n.594-209C=
NR_073010.2:n.1048+8643G= (PTCHD1-AS)
XM_011545536.2:c.594-209C= (PHEX)	XP_011543838.1:n.594-209C=
XM_017029579.1:c.945-209C= (PHEX)	XP_016885068.1:n.945-209C=
XM_024452390.1:c.1410-209C= (PHEX)	XP_024308158.1:n.1410-209C=
XR_001755695.1:n.2541-209C= (PHEX)
NM_000444.6:c.1701-209C= (PHEX) MANE Select	NP_000435.3:n.1701-209C=
NM_001282754.2:c.1701-209C= (PHEX)	NP_001269683.1:n.1701-209C=