Canonical Allele Identifier: CA2419161802
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22077564C= , CM000685.2:g.22077564C= GRCh38
NC_000023.10:g.22095682C= , CM000685.1:g.22095682C= GRCh37
NC_000023.9:g.22005603C= NCBI36
NG_007563.2:g.49762C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.951C=
ENST00000683214.1:n.633C=
ENST00000684143.1:c.522C= ENSP00000508264.1:p.Gly174=
ENST00000684745.1:n.199C=
ENST00000379374.5:c.525C= MANE Select ENSP00000368682.4:p.Gly175=
ENST00000379374.4:c.525C= ENSP00000368682.4:p.Gly175=
NM_000444.5:c.525C= NP_000435.3:p.Gly175=
NM_001282754.1:c.525C= NP_001269683.1:p.Gly175=
XM_011545535.1:c.525C= XP_011543837.1:p.Gly175=
XM_017029579.1:c.-93-12865C= XP_016885068.1:n.-93-12865C=
XM_024452390.1:c.234C= XP_024308158.1:p.Gly78=
XR_001755695.1:n.1204C=
NM_000444.6:c.525C= MANE Select NP_000435.3:p.Gly175=
NM_001282754.2:c.525C= NP_001269683.1:p.Gly175=