Canonical Allele Identifier: CA2419152376
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047148G= , CM000685.2:g.22047148G= GRCh38
NC_000023.10:g.22065266G= , CM000685.1:g.22065266G= GRCh37
NC_000023.9:g.21975187G= NCBI36
NG_007563.2:g.19346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.712G=
ENST00000683214.1:n.544+14025G=
ENST00000684143.1:c.286G= ENSP00000508264.1:p.Glu96=
ENST00000379374.5:c.286G= MANE Select ENSP00000368682.4:p.Glu96=
ENST00000379374.4:c.286G= ENSP00000368682.4:p.Glu96=
NM_000444.5:c.286G= NP_000435.3:p.Glu96=
NM_001282754.1:c.286G= NP_001269683.1:p.Glu96=
XM_011545535.1:c.286G= XP_011543837.1:p.Glu96=
XM_024452390.1:c.-6G= XP_024308158.1:n.-6G=
XR_001755695.1:n.965G=
NM_000444.6:c.286G= MANE Select NP_000435.3:p.Glu96=
NM_001282754.2:c.286G= NP_001269683.1:p.Glu96=