Canonical Allele Identifier: CA369192792
Gene: FLNC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843422A>C , CM000669.2:g.128843422A>C GRCh38
NC_000007.13:g.128483476A>C , CM000669.1:g.128483476A>C GRCh37
NC_000007.12:g.128270712A>C NCBI36
NG_011807.1:g.17994A>C , LRG_870:g.17994A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2656A>C MANE Select ENSP00000327145.8:p.Lys886Gln
ENST00000325888.12:c.2656A>C ENSP00000327145.8:p.Lys886Gln
ENST00000346177.6:c.2656A>C ENSP00000344002.6:p.Lys886Gln
NM_001127487.1:c.2656A>C NP_001120959.1:p.Lys886Gln
NM_001458.4:c.2656A>C , LRG_870t1:c.2656A>C NP_001449.3:p.Lys886Gln
NM_001127487.2:c.2656A>C NP_001120959.1:p.Lys886Gln
NM_001458.5:c.2656A>C MANE Select NP_001449.3:p.Lys886Gln