Canonical Allele Identifier: CA2419152359
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047111C= , CM000685.2:g.22047111C= GRCh38
NC_000023.10:g.22065229C= , CM000685.1:g.22065229C= GRCh37
NC_000023.9:g.21975150C= NCBI36
NG_007563.2:g.19309C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.675C=
ENST00000683214.1:n.544+13988C=
ENST00000684143.1:c.249C= ENSP00000508264.1:p.Phe83=
ENST00000379374.5:c.249C= MANE Select ENSP00000368682.4:p.Phe83=
ENST00000379374.4:c.249C= ENSP00000368682.4:p.Phe83=
NM_000444.5:c.249C= NP_000435.3:p.Phe83=
NM_001282754.1:c.249C= NP_001269683.1:p.Phe83=
XM_011545535.1:c.249C= XP_011543837.1:p.Phe83=
XM_024452390.1:c.-43C= XP_024308158.1:n.-43C=
XR_001755695.1:n.928C=
NM_000444.6:c.249C= MANE Select NP_000435.3:p.Phe83=
NM_001282754.2:c.249C= NP_001269683.1:p.Phe83=