Canonical Allele Identifier: CA2419206668

Gene: PHEX PTCHD1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22212848G= , CM000685.2:g.22212848G=	GRCh38
NC_000023.10:g.22230965G= , CM000685.1:g.22230965G=	GRCh37
NC_000023.9:g.22140886G=	NCBI36
NG_007563.2:g.185045G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682888.1:c.200-56G= (PHEX)	ENSP00000508003.1:n.200-56G=
ENST00000683162.1:c.200-56G= (PHEX)	ENSP00000508059.1:n.200-56G=
ENST00000683289.1:c.200-56G= (PHEX)	ENSP00000508195.1:n.200-56G=
ENST00000683917.1:n.430-56G= (PHEX)
ENST00000684356.1:c.200-56G= (PHEX)	ENSP00000507619.1:n.200-56G=
ENST00000684745.1:n.1320-56G= (PHEX)
ENST00000379374.5:c.1646-56G= (PHEX) MANE Select	ENSP00000368682.4:n.1646-56G=
ENST00000379374.4:c.1646-56G= (PHEX)	ENSP00000368682.4:n.1646-56G=
NM_000444.5:c.1646-56G= (PHEX)	NP_000435.3:n.1646-56G=
NM_001282754.1:c.1646-56G= (PHEX)	NP_001269683.1:n.1646-56G=
XM_011545533.1:c.890-56G= (PHEX)	XP_011543835.1:n.890-56G=
XM_011545534.1:c.890-56G= (PHEX)	XP_011543836.1:n.890-56G=
XM_011545536.1:c.539-56G= (PHEX)	XP_011543838.1:n.539-56G=
NR_073010.2:n.1049-10078C= (PTCHD1-AS)
XM_011545536.2:c.539-56G= (PHEX)	XP_011543838.1:n.539-56G=
XM_017029579.1:c.890-56G= (PHEX)	XP_016885068.1:n.890-56G=
XM_024452390.1:c.1355-56G= (PHEX)	XP_024308158.1:n.1355-56G=
XR_001755695.1:n.2486-56G= (PHEX)
NM_000444.6:c.1646-56G= (PHEX) MANE Select	NP_000435.3:n.1646-56G=
NM_001282754.2:c.1646-56G= (PHEX)	NP_001269683.1:n.1646-56G=