Canonical Allele Identifier: CA2013130380
Gene: FGF23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372578_4372579delinsCA , CM000674.2:g.4372578_4372579delinsCA GRCh38
NC_000012.11:g.4481744_4481745delinsCA , CM000674.1:g.4481744_4481745delinsCA GRCh37
NC_000012.10:g.4352005_4352006delinsCA NCBI36
NG_007087.1:g.12150_12151delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.315+15_315+16delinsTG MANE Select ENSP00000237837.1:n.315+15_315+16delinsTG
ENST00000648100.1:c.*1967+6296_*1967+6297delinsCA ENSP00000497536.1:n.*1967+6296_*1967+6297delinsCA
ENST00000648269.1:n.1815+15_1815+16delinsTG
ENST00000674624.1:c.*1204+6296_*1204+6297delinsCA ENSP00000501898.1:n.*1204+6296_*1204+6297delinsCA
ENST00000237837.1:c.315+15_315+16delinsTG ENSP00000237837.1:n.315+15_315+16delinsTG
NM_020638.2:c.315+15_315+16delinsTG NP_065689.1:n.315+15_315+16delinsTG
NM_020638.3:c.315+15_315+16delinsTG MANE Select NP_065689.1:n.315+15_315+16delinsTG