Canonical Allele Identifier: CA1742569522

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841337_128841338delinsGC , CM000669.2:g.128841337_128841338delinsGC	GRCh38
NC_000007.13:g.128481391_128481392delinsGC , CM000669.1:g.128481391_128481392delinsGC	GRCh37
NC_000007.12:g.128268627_128268628delinsGC	NCBI36
NG_011807.1:g.15909_15910delinsGC , LRG_870:g.15909_15910delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1981_1982delinsGC MANE Select	ENSP00000327145.8:p.Ala661=
ENST00000325888.12:c.1981_1982delinsGC	ENSP00000327145.8:p.Ala661=
ENST00000346177.6:c.1981_1982delinsGC	ENSP00000344002.6:p.Ala661=
ENST00000388853.3:n.7_8delinsGC
NM_001127487.1:c.1981_1982delinsGC	NP_001120959.1:p.Ala661=
NM_001458.4:c.1981_1982delinsGC , LRG_870t1:c.1981_1982delinsGC	NP_001449.3:p.Ala661=
NM_001127487.2:c.1981_1982delinsGC	NP_001120959.1:p.Ala661=
NM_001458.5:c.1981_1982delinsGC MANE Select	NP_001449.3:p.Ala661=