Canonical Allele Identifier: CA515431810

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22196434T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178317T>A , CM000685.2:g.22178317T>A	GRCh38
NC_000023.10:g.22196434T>A , CM000685.1:g.22196434T>A	GRCh37
NC_000023.9:g.22106355T>A	NCBI36
NG_007563.2:g.150514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.81T>A	ENSP00000508003.1:p.Thr27=
ENST00000683162.1:c.81T>A	ENSP00000508059.1:p.Thr27=
ENST00000683289.1:c.81T>A	ENSP00000508195.1:p.Thr27=
ENST00000683917.1:n.311T>A
ENST00000684356.1:c.81T>A	ENSP00000507619.1:p.Thr27=
ENST00000684745.1:n.1201T>A
ENST00000379374.5:c.1527T>A MANE Select	ENSP00000368682.4:p.Thr509=
ENST00000379374.4:c.1527T>A	ENSP00000368682.4:p.Thr509=
NM_000444.5:c.1527T>A	NP_000435.3:p.Thr509=
NM_001282754.1:c.1527T>A	NP_001269683.1:p.Thr509=
XM_011545533.1:c.771T>A	XP_011543835.1:p.Thr257=
XM_011545534.1:c.771T>A	XP_011543836.1:p.Thr257=
XM_011545536.1:c.420T>A	XP_011543838.1:p.Thr140=
XM_011545536.2:c.420T>A	XP_011543838.1:p.Thr140=
XM_017029579.1:c.771T>A	XP_016885068.1:p.Thr257=
XM_024452390.1:c.1236T>A	XP_024308158.1:p.Thr412=
XR_001755695.1:n.2367T>A
NM_000444.6:c.1527T>A MANE Select	NP_000435.3:p.Thr509=
NM_001282754.2:c.1527T>A	NP_001269683.1:p.Thr509=