Canonical Allele Identifier: CA369201880
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1808632986

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847981A>T , CM000669.2:g.128847981A>T GRCh38
NC_000007.13:g.128488035A>T , CM000669.1:g.128488035A>T GRCh37
NC_000007.12:g.128275271A>T NCBI36
NG_011807.1:g.22553A>T , LRG_870:g.22553A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4493A>T MANE Select ENSP00000327145.8:p.Asp1498Val
ENST00000325888.12:c.4493A>T ENSP00000327145.8:p.Asp1498Val
ENST00000346177.6:c.4493A>T ENSP00000344002.6:p.Asp1498Val
NM_001127487.1:c.4493A>T NP_001120959.1:p.Asp1498Val
NM_001458.4:c.4493A>T , LRG_870t1:c.4493A>T NP_001449.3:p.Asp1498Val
NM_001127487.2:c.4493A>T NP_001120959.1:p.Asp1498Val
NM_001458.5:c.4493A>T MANE Select NP_001449.3:p.Asp1498Val