Canonical Allele Identifier: CA2419147563
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22033081T= , CM000685.2:g.22033081T= GRCh38
NC_000023.10:g.22051199T= , CM000685.1:g.22051199T= GRCh37
NC_000023.9:g.21961120T= NCBI36
NG_007563.2:g.5279T=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.502T=
ENST00000683214.1:n.502T=
ENST00000684143.1:c.76T= ENSP00000508264.1:p.Phe26=
ENST00000379374.5:c.76T= MANE Select ENSP00000368682.4:p.Phe26=
ENST00000379374.4:c.76T= ENSP00000368682.4:p.Phe26=
NM_000444.5:c.76T= NP_000435.3:p.Phe26=
NM_001282754.1:c.76T= NP_001269683.1:p.Phe26=
XM_011545535.1:c.76T= XP_011543837.1:p.Phe26=
XR_001755695.1:n.755T=
NM_000444.6:c.76T= MANE Select NP_000435.3:p.Phe26=
NM_001282754.2:c.76T= NP_001269683.1:p.Phe26=