Canonical Allele Identifier: CA4474467
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 471987
dbSNP Id: rs374132023

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840914T>C , CM000669.2:g.128840914T>C GRCh38
NC_000007.13:g.128480968T>C , CM000669.1:g.128480968T>C GRCh37
NC_000007.12:g.128268204T>C NCBI36
NG_011807.1:g.15486T>C , LRG_870:g.15486T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1757T>C MANE Select ENSP00000327145.8:p.Val586Ala
ENST00000325888.12:c.1757T>C ENSP00000327145.8:p.Val586Ala
ENST00000346177.6:c.1757T>C ENSP00000344002.6:p.Val586Ala
NM_001127487.1:c.1757T>C NP_001120959.1:p.Val586Ala
NM_001458.4:c.1757T>C , LRG_870t1:c.1757T>C NP_001449.3:p.Val586Ala
NM_001127487.2:c.1757T>C NP_001120959.1:p.Val586Ala
NM_001458.5:c.1757T>C MANE Select NP_001449.3:p.Val586Ala