Canonical Allele Identifier: CA2419152366
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047125G= , CM000685.2:g.22047125G= GRCh38
NC_000023.10:g.22065243G= , CM000685.1:g.22065243G= GRCh37
NC_000023.9:g.21975164G= NCBI36
NG_007563.2:g.19323G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.689G=
ENST00000683214.1:n.544+14002G=
ENST00000684143.1:c.263G= ENSP00000508264.1:p.Trp88=
ENST00000379374.5:c.263G= MANE Select ENSP00000368682.4:p.Trp88=
ENST00000379374.4:c.263G= ENSP00000368682.4:p.Trp88=
NM_000444.5:c.263G= NP_000435.3:p.Trp88=
NM_001282754.1:c.263G= NP_001269683.1:p.Trp88=
XM_011545535.1:c.263G= XP_011543837.1:p.Trp88=
XM_024452390.1:c.-29G= XP_024308158.1:n.-29G=
XR_001755695.1:n.942G=
NM_000444.6:c.263G= MANE Select NP_000435.3:p.Trp88=
NM_001282754.2:c.263G= NP_001269683.1:p.Trp88=