Canonical Allele Identifier: CA1107054656
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1219695744

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835159A>G , CM000669.2:g.128835159A>G GRCh38
NC_000007.13:g.128475213A>G , CM000669.1:g.128475213A>G GRCh37
NC_000007.12:g.128262449A>G NCBI36
NG_011807.1:g.9731A>G , LRG_870:g.9731A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-167A>G MANE Select ENSP00000327145.8:n.353-167A>G
ENST00000325888.12:c.353-167A>G ENSP00000327145.8:n.353-167A>G
ENST00000346177.6:c.353-167A>G ENSP00000344002.6:n.353-167A>G
NM_001127487.1:c.353-167A>G NP_001120959.1:n.353-167A>G
NM_001458.4:c.353-167A>G , LRG_870t1:c.353-167A>G NP_001449.3:n.353-167A>G
NM_001127487.2:c.353-167A>G NP_001120959.1:n.353-167A>G
NM_001458.5:c.353-167A>G MANE Select NP_001449.3:n.353-167A>G