Canonical Allele Identifier: CA2579571776
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032994del , CM000685.2:g.22032994del GRCh38
NC_000023.10:g.22051112del , CM000685.1:g.22051112del GRCh37
NC_000023.9:g.21961033del NCBI36
NG_007563.2:g.5192del

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.415del
ENST00000683214.1:n.415del
ENST00000684143.1:c.-12del ENSP00000508264.1:n.-12del
ENST00000379374.5:c.-12del MANE Select ENSP00000368682.4:n.-12del
ENST00000379374.4:c.-12del ENSP00000368682.4:n.-12del
NM_000444.5:c.-12del NP_000435.3:n.-12del
NM_001282754.1:c.-12del NP_001269683.1:n.-12del
XM_011545535.1:c.-12del XP_011543837.1:n.-12del
XR_001755695.1:n.668del
NM_000444.6:c.-12del MANE Select NP_000435.3:n.-12del
NM_001282754.2:c.-12del NP_001269683.1:n.-12del