Canonical Allele Identifier: CA515431876

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22208582T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22190465T>C , CM000685.2:g.22190465T>C	GRCh38
NC_000023.10:g.22208582T>C , CM000685.1:g.22208582T>C	GRCh37
NC_000023.9:g.22118503T>C	NCBI36
NG_007563.2:g.162662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.162T>C	ENSP00000508003.1:p.Thr54=
ENST00000683162.1:c.162T>C	ENSP00000508059.1:p.Thr54=
ENST00000683289.1:c.162T>C	ENSP00000508195.1:p.Thr54=
ENST00000683917.1:n.392T>C
ENST00000684356.1:c.162T>C	ENSP00000507619.1:p.Thr54=
ENST00000684745.1:n.1282T>C
ENST00000379374.5:c.1608T>C MANE Select	ENSP00000368682.4:p.Thr536=
ENST00000379374.4:c.1608T>C	ENSP00000368682.4:p.Thr536=
NM_000444.5:c.1608T>C	NP_000435.3:p.Thr536=
NM_001282754.1:c.1608T>C	NP_001269683.1:p.Thr536=
XM_011545533.1:c.852T>C	XP_011543835.1:p.Thr284=
XM_011545534.1:c.852T>C	XP_011543836.1:p.Thr284=
XM_011545536.1:c.501T>C	XP_011543838.1:p.Thr167=
XM_011545536.2:c.501T>C	XP_011543838.1:p.Thr167=
XM_017029579.1:c.852T>C	XP_016885068.1:p.Thr284=
XM_024452390.1:c.1317T>C	XP_024308158.1:p.Thr439=
XR_001755695.1:n.2448T>C
NM_000444.6:c.1608T>C MANE Select	NP_000435.3:p.Thr536=
NM_001282754.2:c.1608T>C	NP_001269683.1:p.Thr536=