Canonical Allele Identifier: CA6395744
Gene: FGF23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372733_4372734insA , CM000674.2:g.4372733_4372734insA GRCh38
NC_000012.11:g.4481899_4481900insA , CM000674.1:g.4481899_4481900insA GRCh37
NC_000012.10:g.4352160_4352161insA NCBI36
NG_007087.1:g.11995_11996insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.212-37_212-36insT MANE Select ENSP00000237837.1:n.212-37_212-36insT
ENST00000648100.1:c.*1967+6451_*1967+6452insA ENSP00000497536.1:n.*1967+6451_*1967+6452insA
ENST00000648269.1:n.1675_1676insT
ENST00000674624.1:c.*1204+6451_*1204+6452insA ENSP00000501898.1:n.*1204+6451_*1204+6452insA
ENST00000237837.1:c.212-37_212-36insT ENSP00000237837.1:n.212-37_212-36insT
NM_020638.2:c.212-37_212-36insT NP_065689.1:n.212-37_212-36insT
NM_020638.3:c.212-37_212-36insT MANE Select NP_065689.1:n.212-37_212-36insT