Canonical Allele Identifier: CA1742580507

Gene: FLNC

Linked Data

• dbSNP Id: rs1808420283

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843354G>A , CM000669.2:g.128843354G>A	GRCh38
NC_000007.13:g.128483408G>A , CM000669.1:g.128483408G>A	GRCh37
NC_000007.12:g.128270644G>A	NCBI36
NG_011807.1:g.17926G>A , LRG_870:g.17926G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2641+35G>A MANE Select	ENSP00000327145.8:n.2641+35G>A
ENST00000325888.12:c.2641+35G>A	ENSP00000327145.8:n.2641+35G>A
ENST00000346177.6:c.2641+35G>A	ENSP00000344002.6:n.2641+35G>A
NM_001127487.1:c.2641+35G>A	NP_001120959.1:n.2641+35G>A
NM_001458.4:c.2641+35G>A , LRG_870t1:c.2641+35G>A	NP_001449.3:n.2641+35G>A
NM_001127487.2:c.2641+35G>A	NP_001120959.1:n.2641+35G>A
NM_001458.5:c.2641+35G>A MANE Select	NP_001449.3:n.2641+35G>A