Canonical Allele Identifier: CA412575566

Gene: PHEX PTCHD1-AS

Linked Data

• ClinVar Variation Id: 861072
• ClinVar RCV Id: RCV001067506
• dbSNP Id: rs1556206403
• MyVariant Identifiers: chrX:g.22266065T>A (hg19) ; chrX:g.22247948T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247948T>A , CM000685.2:g.22247948T>A	GRCh38
NC_000023.10:g.22266065T>A , CM000685.1:g.22266065T>A	GRCh37
NC_000023.9:g.22175986T>A	NCBI36
NG_007563.2:g.220145T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*183T>A (PHEX)	ENSP00000508059.1:n.*183T>A
ENST00000683289.1:c.624+20337T>A (PHEX)	ENSP00000508195.1:n.624+20337T>A
ENST00000683917.1:n.1029T>A (PHEX)
ENST00000684356.1:c.799T>A (PHEX)	ENSP00000507619.1:p.Trp267Arg
ENST00000684745.1:n.1919T>A (PHEX)
ENST00000379374.5:c.2245T>A (PHEX) MANE Select	ENSP00000368682.4:p.Trp749Arg
ENST00000379374.4:c.2245T>A (PHEX)	ENSP00000368682.4:p.Trp749Arg
NM_000444.5:c.2245T>A (PHEX)	NP_000435.3:p.Trp749Arg
NM_001282754.1:c.*80T>A (PHEX)	NP_001269683.1:n.*80T>A
XM_011545533.1:c.1489T>A (PHEX)	XP_011543835.1:p.Trp497Arg
XM_011545534.1:c.1489T>A (PHEX)	XP_011543836.1:p.Trp497Arg
XM_011545536.1:c.1138T>A (PHEX)	XP_011543838.1:p.Trp380Arg
XR_950533.1:n.140+5991A>T
XR_950534.1:n.127+5991A>T
NR_073010.2:n.850+5991A>T (PTCHD1-AS)
XM_011545536.2:c.1138T>A (PHEX)	XP_011543838.1:p.Trp380Arg
XM_017029579.1:c.1489T>A (PHEX)	XP_016885068.1:p.Trp497Arg
XM_024452390.1:c.1954T>A (PHEX)	XP_024308158.1:p.Trp652Arg
XR_001755695.1:n.3085T>A (PHEX)
NM_000444.6:c.2245T>A (PHEX) MANE Select	NP_000435.3:p.Trp749Arg
NM_001282754.2:c.*80T>A (PHEX)	NP_001269683.1:n.*80T>A