Canonical Allele Identifier: CA1742550659

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857437_128857448delinsATCATGGTCAGT , CM000669.2:g.128857437_128857448delinsATCATGGTCAGT	GRCh38
NC_000007.13:g.128497491_128497502delinsATCATGGTCAGT , CM000669.1:g.128497491_128497502delinsATCATGGTCAGT	GRCh37
NC_000007.12:g.128284727_128284738delinsATCATGGTCAGT	NCBI36
NG_011807.1:g.32009_32020delinsATCATGGTCAGT , LRG_870:g.32009_32020delinsATCATGGTCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+101_7780+112delinsATCATGGTCAGT (FLNC) MANE Select	ENSP00000327145.8:n.7780+101_7780+112delinsATCATGGTCAGT
ENST00000325888.12:c.7780+101_7780+112delinsATCATGGTCAGT (FLNC)	ENSP00000327145.8:n.7780+101_7780+112delinsATCATGGTCAGT
ENST00000346177.6:c.7681+101_7681+112delinsATCATGGTCAGT (FLNC)	ENSP00000344002.6:n.7681+101_7681+112delinsATCATGGTCAGT
NM_001127487.1:c.7681+101_7681+112delinsATCATGGTCAGT (FLNC)	NP_001120959.1:n.7681+101_7681+112delinsATCATGGTCAGT
NM_001458.4:c.7780+101_7780+112delinsATCATGGTCAGT , LRG_870t1:c.7780+101_7780+112delinsATCATGGTCAGT (FLNC)	NP_001449.3:n.7780+101_7780+112delinsATCATGGTCAGT
NR_149055.1:n.103-4051_103-4040delinsACTGACCATGAT (FLNC-AS1)
NM_001127487.2:c.7681+101_7681+112delinsATCATGGTCAGT (FLNC)	NP_001120959.1:n.7681+101_7681+112delinsATCATGGTCAGT
NM_001458.5:c.7780+101_7780+112delinsATCATGGTCAGT (FLNC) MANE Select	NP_001449.3:n.7780+101_7780+112delinsATCATGGTCAGT