Canonical Allele Identifier: CA412575517

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22266043A>T (hg19) ; chrX:g.22247926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247926A>T , CM000685.2:g.22247926A>T	GRCh38
NC_000023.10:g.22266043A>T , CM000685.1:g.22266043A>T	GRCh37
NC_000023.9:g.22175964A>T	NCBI36
NG_007563.2:g.220123A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*161A>T (PHEX)	ENSP00000508059.1:n.*161A>T
ENST00000683289.1:c.624+20315A>T (PHEX)	ENSP00000508195.1:n.624+20315A>T
ENST00000683917.1:n.1007A>T (PHEX)
ENST00000684356.1:c.777A>T (PHEX)	ENSP00000507619.1:p.Arg259Ser
ENST00000684745.1:n.1897A>T (PHEX)
ENST00000379374.5:c.2223A>T (PHEX) MANE Select	ENSP00000368682.4:p.Arg741Ser
ENST00000379374.4:c.2223A>T (PHEX)	ENSP00000368682.4:p.Arg741Ser
NM_000444.5:c.2223A>T (PHEX)	NP_000435.3:p.Arg741Ser
NM_001282754.1:c.*58A>T (PHEX)	NP_001269683.1:n.*58A>T
XM_011545533.1:c.1467A>T (PHEX)	XP_011543835.1:p.Arg489Ser
XM_011545534.1:c.1467A>T (PHEX)	XP_011543836.1:p.Arg489Ser
XM_011545536.1:c.1116A>T (PHEX)	XP_011543838.1:p.Arg372Ser
XR_950533.1:n.140+6013T>A
XR_950534.1:n.127+6013T>A
NR_073010.2:n.850+6013T>A (PTCHD1-AS)
XM_011545536.2:c.1116A>T (PHEX)	XP_011543838.1:p.Arg372Ser
XM_017029579.1:c.1467A>T (PHEX)	XP_016885068.1:p.Arg489Ser
XM_024452390.1:c.1932A>T (PHEX)	XP_024308158.1:p.Arg644Ser
XR_001755695.1:n.3063A>T (PHEX)
NM_000444.6:c.2223A>T (PHEX) MANE Select	NP_000435.3:p.Arg741Ser
NM_001282754.2:c.*58A>T (PHEX)	NP_001269683.1:n.*58A>T