Canonical Allele Identifier: CA515431246

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22266034G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247917G>C , CM000685.2:g.22247917G>C	GRCh38
NC_000023.10:g.22266034G>C , CM000685.1:g.22266034G>C	GRCh37
NC_000023.9:g.22175955G>C	NCBI36
NG_007563.2:g.220114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*152G>C (PHEX)	ENSP00000508059.1:n.*152G>C
ENST00000683289.1:c.624+20306G>C (PHEX)	ENSP00000508195.1:n.624+20306G>C
ENST00000683917.1:n.998G>C (PHEX)
ENST00000684356.1:c.768G>C (PHEX)	ENSP00000507619.1:p.Thr256=
ENST00000684745.1:n.1888G>C (PHEX)
ENST00000379374.5:c.2214G>C (PHEX) MANE Select	ENSP00000368682.4:p.Thr738=
ENST00000379374.4:c.2214G>C (PHEX)	ENSP00000368682.4:p.Thr738=
NM_000444.5:c.2214G>C (PHEX)	NP_000435.3:p.Thr738=
NM_001282754.1:c.*49G>C (PHEX)	NP_001269683.1:n.*49G>C
XM_011545533.1:c.1458G>C (PHEX)	XP_011543835.1:p.Thr486=
XM_011545534.1:c.1458G>C (PHEX)	XP_011543836.1:p.Thr486=
XM_011545536.1:c.1107G>C (PHEX)	XP_011543838.1:p.Thr369=
XR_950533.1:n.140+6022C>G
XR_950534.1:n.127+6022C>G
NR_073010.2:n.850+6022C>G (PTCHD1-AS)
XM_011545536.2:c.1107G>C (PHEX)	XP_011543838.1:p.Thr369=
XM_017029579.1:c.1458G>C (PHEX)	XP_016885068.1:p.Thr486=
XM_024452390.1:c.1923G>C (PHEX)	XP_024308158.1:p.Thr641=
XR_001755695.1:n.3054G>C (PHEX)
NM_000444.6:c.2214G>C (PHEX) MANE Select	NP_000435.3:p.Thr738=
NM_001282754.2:c.*49G>C (PHEX)	NP_001269683.1:n.*49G>C