Canonical Allele Identifier: CA2684815355

Gene: FLNC

Linked Data

• gnomAD v4: 7-128843053-GACATGGTGGAGCCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843056_128843070del , CM000669.2:g.128843056_128843070del	GRCh38
NC_000007.13:g.128483110_128483124del , CM000669.1:g.128483110_128483124del	GRCh37
NC_000007.12:g.128270346_128270360del	NCBI36
NG_011807.1:g.17628_17642del , LRG_870:g.17628_17642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2550+102_2550+116del MANE Select	ENSP00000327145.8:n.2550+102_2550+116del
ENST00000325888.12:c.2550+102_2550+116del	ENSP00000327145.8:n.2550+102_2550+116del
ENST00000346177.6:c.2550+102_2550+116del	ENSP00000344002.6:n.2550+102_2550+116del
NM_001127487.1:c.2550+102_2550+116del	NP_001120959.1:n.2550+102_2550+116del
NM_001458.4:c.2550+102_2550+116del , LRG_870t1:c.2550+102_2550+116del	NP_001449.3:n.2550+102_2550+116del
NM_001127487.2:c.2550+102_2550+116del	NP_001120959.1:n.2550+102_2550+116del
NM_001458.5:c.2550+102_2550+116del MANE Select	NP_001449.3:n.2550+102_2550+116del