Canonical Allele Identifier: CA2419152263
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22046769G= , CM000685.2:g.22046769G= GRCh38
NC_000023.10:g.22064887G= , CM000685.1:g.22064887G= GRCh37
NC_000023.9:g.21974808G= NCBI36
NG_007563.2:g.18967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-281G=
ENST00000683214.1:n.544+13646G=
ENST00000684143.1:c.188-281G= ENSP00000508264.1:n.188-281G=
ENST00000379374.5:c.188-281G= MANE Select ENSP00000368682.4:n.188-281G=
ENST00000379374.4:c.188-281G= ENSP00000368682.4:n.188-281G=
NM_000444.5:c.188-281G= NP_000435.3:n.188-281G=
NM_001282754.1:c.188-281G= NP_001269683.1:n.188-281G=
XM_011545535.1:c.188-281G= XP_011543837.1:n.188-281G=
XM_024452390.1:c.-104-281G= XP_024308158.1:n.-104-281G=
XR_001755695.1:n.867-281G=
NM_000444.6:c.188-281G= MANE Select NP_000435.3:n.188-281G=
NM_001282754.2:c.188-281G= NP_001269683.1:n.188-281G=