Canonical Allele Identifier: CA2617166857
Gene: FGF23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372604dup , CM000674.2:g.4372604dup GRCh38
NC_000012.11:g.4481770dup , CM000674.1:g.4481770dup GRCh37
NC_000012.10:g.4352031dup NCBI36
NG_007087.1:g.12129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.309dup MANE Select ENSP00000237837.1:p.Gly104TrpfsTer?
ENST00000648100.1:c.*1967+6322dup ENSP00000497536.1:n.*1967+6322dup
ENST00000648269.1:n.1809dup
ENST00000674624.1:c.*1204+6322dup ENSP00000501898.1:n.*1204+6322dup
ENST00000237837.1:c.309dup ENSP00000237837.1:p.Gly104TrpfsTer?
NM_020638.2:c.309dup NP_065689.1:p.Gly104TrpfsTer?
NM_020638.3:c.309dup MANE Select NP_065689.1:p.Gly104TrpfsTer?