Canonical Allele Identifier: CA2515575102
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22096815del , CM000685.2:g.22096815del GRCh38
NC_000023.10:g.22114933del , CM000685.1:g.22114933del GRCh37
NC_000023.9:g.22024854del NCBI36
NG_007563.2:g.69013del

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.1276-140del
ENST00000684143.1:c.847-140del ENSP00000508264.1:n.847-140del
ENST00000684745.1:n.524-140del
ENST00000379374.5:c.850-140del MANE Select ENSP00000368682.4:n.850-140del
ENST00000379374.4:c.850-140del ENSP00000368682.4:n.850-140del
ENST00000475778.1:n.123-140del
NM_000444.5:c.850-140del NP_000435.3:n.850-140del
NM_001282754.1:c.850-140del NP_001269683.1:n.850-140del
XM_011545533.1:c.94-140del XP_011543835.1:n.94-140del
XM_011545534.1:c.94-140del XP_011543836.1:n.94-140del
XM_011545535.1:c.850-140del XP_011543837.1:n.850-140del
XM_017029579.1:c.94-140del XP_016885068.1:n.94-140del
XM_024452390.1:c.559-140del XP_024308158.1:n.559-140del
XR_001755695.1:n.1529-140del
NM_000444.6:c.850-140del MANE Select NP_000435.3:n.850-140del
NM_001282754.2:c.850-140del NP_001269683.1:n.850-140del