Canonical Allele Identifier: CA369191646
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs2128935765

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842856G>C , CM000669.2:g.128842856G>C GRCh38
NC_000007.13:g.128482910G>C , CM000669.1:g.128482910G>C GRCh37
NC_000007.12:g.128270146G>C NCBI36
NG_011807.1:g.17428G>C , LRG_870:g.17428G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2452G>C MANE Select ENSP00000327145.8:p.Asp818His
ENST00000325888.12:c.2452G>C ENSP00000327145.8:p.Asp818His
ENST00000346177.6:c.2452G>C ENSP00000344002.6:p.Asp818His
ENST00000388853.3:n.568G>C
NM_001127487.1:c.2452G>C NP_001120959.1:p.Asp818His
NM_001458.4:c.2452G>C , LRG_870t1:c.2452G>C NP_001449.3:p.Asp818His
NM_001127487.2:c.2452G>C NP_001120959.1:p.Asp818His
NM_001458.5:c.2452G>C MANE Select NP_001449.3:p.Asp818His