Canonical Allele Identifier: CA2693303898
Gene: PHEX HGNC NCBI

Linked Data

gnomAD v4: X-22032980-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032980C>A , CM000685.2:g.22032980C>A GRCh38
NC_000023.10:g.22051098C>A , CM000685.1:g.22051098C>A GRCh37
NC_000023.9:g.21961019C>A NCBI36
NG_007563.2:g.5178C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.401C>A
ENST00000683214.1:n.401C>A
ENST00000684143.1:c.-26C>A ENSP00000508264.1:n.-26C>A
ENST00000379374.5:c.-26C>A MANE Select ENSP00000368682.4:n.-26C>A
ENST00000379374.4:c.-26C>A ENSP00000368682.4:n.-26C>A
NM_000444.5:c.-26C>A NP_000435.3:n.-26C>A
NM_001282754.1:c.-26C>A NP_001269683.1:n.-26C>A
XM_011545535.1:c.-26C>A XP_011543837.1:n.-26C>A
XR_001755695.1:n.654C>A
NM_000444.6:c.-26C>A MANE Select NP_000435.3:n.-26C>A
NM_001282754.2:c.-26C>A NP_001269683.1:n.-26C>A
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