Canonical Allele Identifier: CA2419152381
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047157C= , CM000685.2:g.22047157C= GRCh38
NC_000023.10:g.22065275C= , CM000685.1:g.22065275C= GRCh37
NC_000023.9:g.21975196C= NCBI36
NG_007563.2:g.19355C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.721C=
ENST00000683214.1:n.544+14034C=
ENST00000684143.1:c.295C= ENSP00000508264.1:p.Pro99=
ENST00000379374.5:c.295C= MANE Select ENSP00000368682.4:p.Pro99=
ENST00000379374.4:c.295C= ENSP00000368682.4:p.Pro99=
NM_000444.5:c.295C= NP_000435.3:p.Pro99=
NM_001282754.1:c.295C= NP_001269683.1:p.Pro99=
XM_011545535.1:c.295C= XP_011543837.1:p.Pro99=
XM_024452390.1:c.4C= XP_024308158.1:p.Pro2=
XR_001755695.1:n.974C=
NM_000444.6:c.295C= MANE Select NP_000435.3:p.Pro99=
NM_001282754.2:c.295C= NP_001269683.1:p.Pro99=