Canonical Allele Identifier: CA2419152347
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047080C= , CM000685.2:g.22047080C= GRCh38
NC_000023.10:g.22065198C= , CM000685.1:g.22065198C= GRCh37
NC_000023.9:g.21975119C= NCBI36
NG_007563.2:g.19278C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.644C=
ENST00000683214.1:n.544+13957C=
ENST00000684143.1:c.218C= ENSP00000508264.1:p.Ser73=
ENST00000379374.5:c.218C= MANE Select ENSP00000368682.4:p.Ser73=
ENST00000379374.4:c.218C= ENSP00000368682.4:p.Ser73=
NM_000444.5:c.218C= NP_000435.3:p.Ser73=
NM_001282754.1:c.218C= NP_001269683.1:p.Ser73=
XM_011545535.1:c.218C= XP_011543837.1:p.Ser73=
XM_024452390.1:c.-74C= XP_024308158.1:n.-74C=
XR_001755695.1:n.897C=
NM_000444.6:c.218C= MANE Select NP_000435.3:p.Ser73=
NM_001282754.2:c.218C= NP_001269683.1:p.Ser73=