Canonical Allele Identifier: CA412575385

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22265988A>C (hg19) ; chrX:g.22247871A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247871A>C , CM000685.2:g.22247871A>C	GRCh38
NC_000023.10:g.22265988A>C , CM000685.1:g.22265988A>C	GRCh37
NC_000023.9:g.22175909A>C	NCBI36
NG_007563.2:g.220068A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683162.1:c.*106A>C (PHEX)	ENSP00000508059.1:n.*106A>C
ENST00000683289.1:c.624+20260A>C (PHEX)	ENSP00000508195.1:n.624+20260A>C
ENST00000683917.1:n.952A>C (PHEX)
ENST00000684356.1:c.722A>C (PHEX)	ENSP00000507619.1:p.Asn241Thr
ENST00000684745.1:n.1842A>C (PHEX)
ENST00000379374.5:c.2168A>C (PHEX) MANE Select	ENSP00000368682.4:p.Asn723Thr
ENST00000379374.4:c.2168A>C (PHEX)	ENSP00000368682.4:p.Asn723Thr
NM_000444.5:c.2168A>C (PHEX)	NP_000435.3:p.Asn723Thr
NM_001282754.1:c.*3A>C (PHEX)	NP_001269683.1:n.*3A>C
XM_011545533.1:c.1412A>C (PHEX)	XP_011543835.1:p.Asn471Thr
XM_011545534.1:c.1412A>C (PHEX)	XP_011543836.1:p.Asn471Thr
XM_011545536.1:c.1061A>C (PHEX)	XP_011543838.1:p.Asn354Thr
XR_950533.1:n.140+6068T>G
XR_950534.1:n.127+6068T>G
NR_073010.2:n.850+6068T>G (PTCHD1-AS)
XM_011545536.2:c.1061A>C (PHEX)	XP_011543838.1:p.Asn354Thr
XM_017029579.1:c.1412A>C (PHEX)	XP_016885068.1:p.Asn471Thr
XM_024452390.1:c.1877A>C (PHEX)	XP_024308158.1:p.Asn626Thr
XR_001755695.1:n.3008A>C (PHEX)
NM_000444.6:c.2168A>C (PHEX) MANE Select	NP_000435.3:p.Asn723Thr
NM_001282754.2:c.*3A>C (PHEX)	NP_001269683.1:n.*3A>C