Canonical Allele Identifier: CA515423861
Gene: PHEX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.22051204C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22033086C>A , CM000685.2:g.22033086C>A GRCh38
NC_000023.10:g.22051204C>A , CM000685.1:g.22051204C>A GRCh37
NC_000023.9:g.21961125C>A NCBI36
NG_007563.2:g.5284C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.507C>A
ENST00000683214.1:n.507C>A
ENST00000684143.1:c.81C>A ENSP00000508264.1:p.Val27=
ENST00000379374.5:c.81C>A MANE Select ENSP00000368682.4:p.Val27=
ENST00000379374.4:c.81C>A ENSP00000368682.4:p.Val27=
NM_000444.5:c.81C>A NP_000435.3:p.Val27=
NM_001282754.1:c.81C>A NP_001269683.1:p.Val27=
XM_011545535.1:c.81C>A XP_011543837.1:p.Val27=
XR_001755695.1:n.760C>A
NM_000444.6:c.81C>A MANE Select NP_000435.3:p.Val27=
NM_001282754.2:c.81C>A NP_001269683.1:p.Val27=
Search 100 bp 5'
Search 100 bp 3'