Canonical Allele Identifier: CA515432028

Gene: PHEX PTCHD1-AS

Linked Data

• gnomAD v4: X-22219081-T-C
• MyVariant Identifiers: chrX:g.22237198T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22219081T>C , CM000685.2:g.22219081T>C	GRCh38
NC_000023.10:g.22237198T>C , CM000685.1:g.22237198T>C	GRCh37
NC_000023.9:g.22147119T>C	NCBI36
NG_007563.2:g.191278T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682888.1:c.300T>C (PHEX)	ENSP00000508003.1:p.Phe100=
ENST00000683162.1:c.300T>C (PHEX)	ENSP00000508059.1:p.Phe100=
ENST00000683289.1:c.300T>C (PHEX)	ENSP00000508195.1:p.Phe100=
ENST00000683917.1:n.530T>C (PHEX)
ENST00000684356.1:c.300T>C (PHEX)	ENSP00000507619.1:p.Phe100=
ENST00000684745.1:n.1420T>C (PHEX)
ENST00000379374.5:c.1746T>C (PHEX) MANE Select	ENSP00000368682.4:p.Phe582=
ENST00000379374.4:c.1746T>C (PHEX)	ENSP00000368682.4:p.Phe582=
NM_000444.5:c.1746T>C (PHEX)	NP_000435.3:p.Phe582=
NM_001282754.1:c.1746T>C (PHEX)	NP_001269683.1:p.Phe582=
XM_011545533.1:c.990T>C (PHEX)	XP_011543835.1:p.Phe330=
XM_011545534.1:c.990T>C (PHEX)	XP_011543836.1:p.Phe330=
XM_011545536.1:c.639T>C (PHEX)	XP_011543838.1:p.Phe213=
NR_073010.2:n.1048+8389A>G (PTCHD1-AS)
XM_011545536.2:c.639T>C (PHEX)	XP_011543838.1:p.Phe213=
XM_017029579.1:c.990T>C (PHEX)	XP_016885068.1:p.Phe330=
XM_024452390.1:c.1455T>C (PHEX)	XP_024308158.1:p.Phe485=
XR_001755695.1:n.2586T>C (PHEX)
NM_000444.6:c.1746T>C (PHEX) MANE Select	NP_000435.3:p.Phe582=
NM_001282754.2:c.1746T>C (PHEX)	NP_001269683.1:p.Phe582=