Canonical Allele Identifier: CA2617166851
Gene: FGF23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372588del , CM000674.2:g.4372588del GRCh38
NC_000012.11:g.4481754del , CM000674.1:g.4481754del GRCh37
NC_000012.10:g.4352015del NCBI36
NG_007087.1:g.12143del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.315+8del MANE Select ENSP00000237837.1:n.315+8del
ENST00000648100.1:c.*1967+6306del ENSP00000497536.1:n.*1967+6306del
ENST00000648269.1:n.1815+8del
ENST00000674624.1:c.*1204+6306del ENSP00000501898.1:n.*1204+6306del
ENST00000237837.1:c.315+8del ENSP00000237837.1:n.315+8del
NM_020638.2:c.315+8del NP_065689.1:n.315+8del
NM_020638.3:c.315+8del MANE Select NP_065689.1:n.315+8del