Canonical Allele Identifier: CA515431836

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22196476A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178359A>G , CM000685.2:g.22178359A>G	GRCh38
NC_000023.10:g.22196476A>G , CM000685.1:g.22196476A>G	GRCh37
NC_000023.9:g.22106397A>G	NCBI36
NG_007563.2:g.150556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.123A>G	ENSP00000508003.1:p.Lys41=
ENST00000683162.1:c.123A>G	ENSP00000508059.1:p.Lys41=
ENST00000683289.1:c.123A>G	ENSP00000508195.1:p.Lys41=
ENST00000683917.1:n.353A>G
ENST00000684356.1:c.123A>G	ENSP00000507619.1:p.Lys41=
ENST00000684745.1:n.1243A>G
ENST00000379374.5:c.1569A>G MANE Select	ENSP00000368682.4:p.Lys523=
ENST00000379374.4:c.1569A>G	ENSP00000368682.4:p.Lys523=
NM_000444.5:c.1569A>G	NP_000435.3:p.Lys523=
NM_001282754.1:c.1569A>G	NP_001269683.1:p.Lys523=
XM_011545533.1:c.813A>G	XP_011543835.1:p.Lys271=
XM_011545534.1:c.813A>G	XP_011543836.1:p.Lys271=
XM_011545536.1:c.462A>G	XP_011543838.1:p.Lys154=
XM_011545536.2:c.462A>G	XP_011543838.1:p.Lys154=
XM_017029579.1:c.813A>G	XP_016885068.1:p.Lys271=
XM_024452390.1:c.1278A>G	XP_024308158.1:p.Lys426=
XR_001755695.1:n.2409A>G
NM_000444.6:c.1569A>G MANE Select	NP_000435.3:p.Lys523=
NM_001282754.2:c.1569A>G	NP_001269683.1:p.Lys523=