Canonical Allele Identifier: CA2580076613
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1997311
ClinVar RCV Id: RCV002823958

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851486_128851487insTGT , CM000669.2:g.128851486_128851487insTGT GRCh38
NC_000007.13:g.128491540_128491541insTGT , CM000669.1:g.128491540_128491541insTGT GRCh37
NC_000007.12:g.128278776_128278777insTGT NCBI36
NG_011807.1:g.26058_26059insTGT , LRG_870:g.26058_26059insTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5700_5701insTGT (FLNC) MANE Select ENSP00000327145.8:p.Ser1900_Lys1901insCys...
ENST00000325888.12:c.5700_5701insTGT (FLNC) ENSP00000327145.8:p.Ser1900_Lys1901insCys...
ENST00000346177.6:c.5601_5602insTGT (FLNC) ENSP00000344002.6:p.Ser1867_Lys1868insCys...
NM_001127487.1:c.5601_5602insTGT (FLNC) NP_001120959.1:p.Ser1867_Lys1868insCys
NM_001458.4:c.5700_5701insTGT , LRG_870t1:c.5700_5701insTGT (FLNC) NP_001449.3:p.Ser1900_Lys1901insCys
NR_149055.1:n.229_230insACA (FLNC-AS1)
NM_001127487.2:c.5601_5602insTGT (FLNC) NP_001120959.1:p.Ser1867_Lys1868insCys
NM_001458.5:c.5700_5701insTGT (FLNC) MANE Select NP_001449.3:p.Ser1900_Lys1901insCys