Canonical Allele Identifier: CA2419147519
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032983G= , CM000685.2:g.22032983G= GRCh38
NC_000023.10:g.22051101G= , CM000685.1:g.22051101G= GRCh37
NC_000023.9:g.21961022G= NCBI36
NG_007563.2:g.5181G=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.404G=
ENST00000683214.1:n.404G=
ENST00000684143.1:c.-23G= ENSP00000508264.1:n.-23G=
ENST00000379374.5:c.-23G= MANE Select ENSP00000368682.4:n.-23G=
ENST00000379374.4:c.-23G= ENSP00000368682.4:n.-23G=
NM_000444.5:c.-23G= NP_000435.3:n.-23G=
NM_001282754.1:c.-23G= NP_001269683.1:n.-23G=
XM_011545535.1:c.-23G= XP_011543837.1:n.-23G=
XR_001755695.1:n.657G=
NM_000444.6:c.-23G= MANE Select NP_000435.3:n.-23G=
NM_001282754.2:c.-23G= NP_001269683.1:n.-23G=