Canonical Allele Identifier: CA2419147468
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032877C= , CM000685.2:g.22032877C= GRCh38
NC_000023.10:g.22050995C= , CM000685.1:g.22050995C= GRCh37
NC_000023.9:g.21960916C= NCBI36
NG_007563.2:g.5075C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.298C=
ENST00000683214.1:n.298C=
ENST00000684143.1:c.-129C= ENSP00000508264.1:n.-129C=
ENST00000379374.5:c.-129C= MANE Select ENSP00000368682.4:n.-129C=
ENST00000379374.4:c.-129C= ENSP00000368682.4:n.-129C=
NM_000444.5:c.-129C= NP_000435.3:n.-129C=
NM_001282754.1:c.-129C= NP_001269683.1:n.-129C=
XM_011545535.1:c.-129C= XP_011543837.1:n.-129C=
XR_001755695.1:n.551C=
NM_000444.6:c.-129C= MANE Select NP_000435.3:n.-129C=
NM_001282754.2:c.-129C= NP_001269683.1:n.-129C=