Canonical Allele Identifier: CA10368352

Gene: PHEX PTCHD1-AS

Linked Data

• dbSNP Id: rs747743987
• ExAC: X:22239755 C / T
• gnomAD v2: X-22239755-C-T
• gnomAD v3: X-22221638-C-T
• gnomAD v4: X-22221638-C-T
• MyVariant Identifiers: chrX:g.22239755C>T (hg19) ; chrX:g.22221638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22221638C>T , CM000685.2:g.22221638C>T	GRCh38
NC_000023.10:g.22239755C>T , CM000685.1:g.22239755C>T	GRCh37
NC_000023.9:g.22149676C>T	NCBI36
NG_007563.2:g.193835C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682888.1:c.348C>T (PHEX)	ENSP00000508003.1:p.Asn116=
ENST00000683162.1:c.348C>T (PHEX)	ENSP00000508059.1:p.Asn116=
ENST00000683289.1:c.348C>T (PHEX)	ENSP00000508195.1:p.Asn116=
ENST00000683917.1:n.578C>T (PHEX)
ENST00000684356.1:c.348C>T (PHEX)	ENSP00000507619.1:p.Asn116=
ENST00000684745.1:n.1468C>T (PHEX)
ENST00000379374.5:c.1794C>T (PHEX) MANE Select	ENSP00000368682.4:p.Asn598=
ENST00000379374.4:c.1794C>T (PHEX)	ENSP00000368682.4:p.Asn598=
NM_000444.5:c.1794C>T (PHEX)	NP_000435.3:p.Asn598=
NM_001282754.1:c.1794C>T (PHEX)	NP_001269683.1:p.Asn598=
XM_011545533.1:c.1038C>T (PHEX)	XP_011543835.1:p.Asn346=
XM_011545534.1:c.1038C>T (PHEX)	XP_011543836.1:p.Asn346=
XM_011545536.1:c.687C>T (PHEX)	XP_011543838.1:p.Asn229=
NR_073010.2:n.1048+5832G>A (PTCHD1-AS)
XM_011545536.2:c.687C>T (PHEX)	XP_011543838.1:p.Asn229=
XM_017029579.1:c.1038C>T (PHEX)	XP_016885068.1:p.Asn346=
XM_024452390.1:c.1503C>T (PHEX)	XP_024308158.1:p.Asn501=
XR_001755695.1:n.2634C>T (PHEX)
NM_000444.6:c.1794C>T (PHEX) MANE Select	NP_000435.3:p.Asn598=
NM_001282754.2:c.1794C>T (PHEX)	NP_001269683.1:p.Asn598=