Canonical Allele Identifier: CA2419220766

Gene: PHEX PTCHD1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22248120G= , CM000685.2:g.22248120G=	GRCh38
NC_000023.10:g.22266237G= , CM000685.1:g.22266237G=	GRCh37
NC_000023.9:g.22176158G=	NCBI36
NG_007563.2:g.220317G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*355G= (PHEX)	ENSP00000508059.1:n.*355G=
ENST00000683289.1:c.624+20509G= (PHEX)	ENSP00000508195.1:n.624+20509G=
ENST00000683917.1:n.1158+43G= (PHEX)
ENST00000684356.1:c.*167G= (PHEX)	ENSP00000507619.1:n.*167G=
ENST00000684745.1:n.2091G= (PHEX)
ENST00000379374.5:c.*167G= (PHEX) MANE Select	ENSP00000368682.4:n.*167G=
ENST00000379374.4:c.*167G= (PHEX)	ENSP00000368682.4:n.*167G=
NM_000444.5:c.*167G= (PHEX)	NP_000435.3:n.*167G=
NM_001282754.1:c.*252G= (PHEX)	NP_001269683.1:n.*252G=
XM_011545533.1:c.*167G= (PHEX)	XP_011543835.1:n.*167G=
XM_011545534.1:c.*167G= (PHEX)	XP_011543836.1:n.*167G=
XM_011545536.1:c.*167G= (PHEX)	XP_011543838.1:n.*167G=
XR_950533.1:n.140+5819C=
XR_950534.1:n.127+5819C=
NR_073010.2:n.850+5819C= (PTCHD1-AS)
XM_011545536.2:c.*167G= (PHEX)	XP_011543838.1:n.*167G=
XM_017029579.1:c.*167G= (PHEX)	XP_016885068.1:n.*167G=
XM_024452390.1:c.*167G= (PHEX)	XP_024308158.1:n.*167G=
XR_001755695.1:n.3257G= (PHEX)
NM_000444.6:c.*167G= (PHEX) MANE Select	NP_000435.3:n.*167G=
NM_001282754.2:c.*252G= (PHEX)	NP_001269683.1:n.*252G=