Canonical Allele Identifier: CA1742552068
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858343_128858346delinsCATG , CM000669.2:g.128858343_128858346delinsCATG GRCh38
NC_000007.13:g.128498397_128498400delinsCATG , CM000669.1:g.128498397_128498400delinsCATG GRCh37
NC_000007.12:g.128285633_128285636delinsCATG NCBI36
NG_011807.1:g.32915_32918delinsCATG , LRG_870:g.32915_32918delinsCATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7998_8001delinsCATG (FLNC) MANE Select ENSP00000327145.8:p.Asn2666=
ENST00000325888.12:c.7998_8001delinsCATG (FLNC) ENSP00000327145.8:p.Asn2666=
ENST00000346177.6:c.7899_7902delinsCATG (FLNC) ENSP00000344002.6:p.Asn2633=
NM_001127487.1:c.7899_7902delinsCATG (FLNC) NP_001120959.1:p.Asn2633=
NM_001458.4:c.7998_8001delinsCATG , LRG_870t1:c.7998_8001delinsCATG (FLNC) NP_001449.3:p.Asn2666=
NR_149055.1:n.102+4179_102+4182delinsCATG (FLNC-AS1)
NM_001127487.2:c.7899_7902delinsCATG (FLNC) NP_001120959.1:p.Asn2633=
NM_001458.5:c.7998_8001delinsCATG (FLNC) MANE Select NP_001449.3:p.Asn2666=