Canonical Allele Identifier: CA515428619

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22094531A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076413A>G , CM000685.2:g.22076413A>G	GRCh38
NC_000023.10:g.22094531A>G , CM000685.1:g.22094531A>G	GRCh37
NC_000023.9:g.22004452A>G	NCBI36
NG_007563.2:g.48611A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.801A>G
ENST00000683214.1:n.545-1063A>G
ENST00000684143.1:c.375A>G	ENSP00000508264.1:p.Arg125=
ENST00000684745.1:n.52A>G
ENST00000379374.5:c.375A>G MANE Select	ENSP00000368682.4:p.Arg125=
ENST00000379374.4:c.375A>G	ENSP00000368682.4:p.Arg125=
NM_000444.5:c.375A>G	NP_000435.3:p.Arg125=
NM_001282754.1:c.375A>G	NP_001269683.1:p.Arg125=
XM_011545535.1:c.375A>G	XP_011543837.1:p.Arg125=
XM_017029579.1:c.-93-14016A>G	XP_016885068.1:n.-93-14016A>G
XM_024452390.1:c.84A>G	XP_024308158.1:p.Arg28=
XR_001755695.1:n.1054A>G
NM_000444.6:c.375A>G MANE Select	NP_000435.3:p.Arg125=
NM_001282754.2:c.375A>G	NP_001269683.1:p.Arg125=