Canonical Allele Identifier: CA1742568845

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841239_128841240delinsTG , CM000669.2:g.128841239_128841240delinsTG	GRCh38
NC_000007.13:g.128481293_128481294delinsTG , CM000669.1:g.128481293_128481294delinsTG	GRCh37
NC_000007.12:g.128268529_128268530delinsTG	NCBI36
NG_011807.1:g.15811_15812delinsTG , LRG_870:g.15811_15812delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1883_1884delinsTG MANE Select	ENSP00000327145.8:p.Val628=
ENST00000325888.12:c.1883_1884delinsTG	ENSP00000327145.8:p.Val628=
ENST00000346177.6:c.1883_1884delinsTG	ENSP00000344002.6:p.Val628=
NM_001127487.1:c.1883_1884delinsTG	NP_001120959.1:p.Val628=
NM_001458.4:c.1883_1884delinsTG , LRG_870t1:c.1883_1884delinsTG	NP_001449.3:p.Val628=
NM_001127487.2:c.1883_1884delinsTG	NP_001120959.1:p.Val628=
NM_001458.5:c.1883_1884delinsTG MANE Select	NP_001449.3:p.Val628=