Canonical Allele Identifier: CA1742545938

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128840126_128840133delinsCAGCGGGG , CM000669.2:g.128840126_128840133delinsCAGCGGGG	GRCh38
NC_000007.13:g.128480180_128480187delinsCAGCGGGG , CM000669.1:g.128480180_128480187delinsCAGCGGGG	GRCh37
NC_000007.12:g.128267416_128267423delinsCAGCGGGG	NCBI36
NG_011807.1:g.14698_14705delinsCAGCGGGG , LRG_870:g.14698_14705delinsCAGCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1515_1522delinsCAGCGGGG MANE Select	ENSP00000327145.8:p.Gly505=
ENST00000325888.12:c.1515_1522delinsCAGCGGGG	ENSP00000327145.8:p.Gly505=
ENST00000346177.6:c.1515_1522delinsCAGCGGGG	ENSP00000344002.6:p.Gly505=
NM_001127487.1:c.1515_1522delinsCAGCGGGG	NP_001120959.1:p.Gly505=
NM_001458.4:c.1515_1522delinsCAGCGGGG , LRG_870t1:c.1515_1522delinsCAGCGGGG	NP_001449.3:p.Gly505=
NM_001127487.2:c.1515_1522delinsCAGCGGGG	NP_001120959.1:p.Gly505=
NM_001458.5:c.1515_1522delinsCAGCGGGG MANE Select	NP_001449.3:p.Gly505=