Canonical Allele Identifier: CA1742566481

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128840987_128840990delinsCAGG , CM000669.2:g.128840987_128840990delinsCAGG	GRCh38
NC_000007.13:g.128481041_128481044delinsCAGG , CM000669.1:g.128481041_128481044delinsCAGG	GRCh37
NC_000007.12:g.128268277_128268280delinsCAGG	NCBI36
NG_011807.1:g.15559_15562delinsCAGG , LRG_870:g.15559_15562delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1813+17_1813+20delinsCAGG MANE Select	ENSP00000327145.8:n.1813+17_1813+20delinsCAGG
ENST00000325888.12:c.1813+17_1813+20delinsCAGG	ENSP00000327145.8:n.1813+17_1813+20delinsCAGG
ENST00000346177.6:c.1813+17_1813+20delinsCAGG	ENSP00000344002.6:n.1813+17_1813+20delinsCAGG
NM_001127487.1:c.1813+17_1813+20delinsCAGG	NP_001120959.1:n.1813+17_1813+20delinsCAGG
NM_001458.4:c.1813+17_1813+20delinsCAGG , LRG_870t1:c.1813+17_1813+20delinsCAGG	NP_001449.3:n.1813+17_1813+20delinsCAGG
NM_001127487.2:c.1813+17_1813+20delinsCAGG	NP_001120959.1:n.1813+17_1813+20delinsCAGG
NM_001458.5:c.1813+17_1813+20delinsCAGG MANE Select	NP_001449.3:n.1813+17_1813+20delinsCAGG