Canonical Allele Identifier: CA2419147469
Gene: PHEX HGNC NCBI

Linked Data

dbSNP Id: rs1926858027

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032879dup , CM000685.2:g.22032879dup GRCh38
NC_000023.10:g.22050997dup , CM000685.1:g.22050997dup GRCh37
NC_000023.9:g.21960918dup NCBI36
NG_007563.2:g.5077dup

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.300dup
ENST00000683214.1:n.300dup
ENST00000684143.1:c.-127dup ENSP00000508264.1:n.-127dup
ENST00000379374.5:c.-127dup MANE Select ENSP00000368682.4:n.-127dup
ENST00000379374.4:c.-127dup ENSP00000368682.4:n.-127dup
NM_000444.5:c.-127dup NP_000435.3:n.-127dup
NM_001282754.1:c.-127dup NP_001269683.1:n.-127dup
XM_011545535.1:c.-127dup XP_011543837.1:n.-127dup
XR_001755695.1:n.553dup
NM_000444.6:c.-127dup MANE Select NP_000435.3:n.-127dup
NM_001282754.2:c.-127dup NP_001269683.1:n.-127dup