Canonical Allele Identifier: CA2579571843
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047037del , CM000685.2:g.22047037del GRCh38
NC_000023.10:g.22065155del , CM000685.1:g.22065155del GRCh37
NC_000023.9:g.21975076del NCBI36
NG_007563.2:g.19235del

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.614-13del
ENST00000683214.1:n.544+13914del
ENST00000684143.1:c.188-13del ENSP00000508264.1:n.188-13del
ENST00000379374.5:c.188-13del MANE Select ENSP00000368682.4:n.188-13del
ENST00000379374.4:c.188-13del ENSP00000368682.4:n.188-13del
NM_000444.5:c.188-13del NP_000435.3:n.188-13del
NM_001282754.1:c.188-13del NP_001269683.1:n.188-13del
XM_011545535.1:c.188-13del XP_011543837.1:n.188-13del
XM_024452390.1:c.-104-13del XP_024308158.1:n.-104-13del
XR_001755695.1:n.867-13del
NM_000444.6:c.188-13del MANE Select NP_000435.3:n.188-13del
NM_001282754.2:c.188-13del NP_001269683.1:n.188-13del