Canonical Allele Identifier: CA2697552891
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 2762362
ClinVar RCV Id: RCV003570035

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047101del , CM000685.2:g.22047101del GRCh38
NC_000023.10:g.22065219del , CM000685.1:g.22065219del GRCh37
NC_000023.9:g.21975140del NCBI36
NG_007563.2:g.19299del

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.665del
ENST00000683214.1:n.544+13978del
ENST00000684143.1:c.239del ENSP00000508264.1:p.Phe80SerfsTer10
ENST00000379374.5:c.239del MANE Select ENSP00000368682.4:p.Phe80SerfsTer10
ENST00000379374.4:c.239del ENSP00000368682.4:p.Phe80SerfsTer10
NM_000444.5:c.239del NP_000435.3:p.Phe80SerfsTer10
NM_001282754.1:c.239del NP_001269683.1:p.Phe80SerfsTer10
XM_011545535.1:c.239del XP_011543837.1:p.Phe80SerfsTer10
XM_024452390.1:c.-53del XP_024308158.1:n.-53del
XR_001755695.1:n.918del
NM_000444.6:c.239del MANE Select NP_000435.3:p.Phe80SerfsTer10
NM_001282754.2:c.239del NP_001269683.1:p.Phe80SerfsTer10