Canonical Allele Identifier: CA2684816293

Gene: FLNC

Linked Data

• gnomAD v4: 7-128843714-AGCTTCAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843715_128843721del , CM000669.2:g.128843715_128843721del	GRCh38
NC_000007.13:g.128483769_128483775del , CM000669.1:g.128483769_128483775del	GRCh37
NC_000007.12:g.128271005_128271011del	NCBI36
NG_011807.1:g.18287_18293del , LRG_870:g.18287_18293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2812-81_2812-75del MANE Select	ENSP00000327145.8:n.2812-81_2812-75del
ENST00000325888.12:c.2812-81_2812-75del	ENSP00000327145.8:n.2812-81_2812-75del
ENST00000346177.6:c.2812-81_2812-75del	ENSP00000344002.6:n.2812-81_2812-75del
NM_001127487.1:c.2812-81_2812-75del	NP_001120959.1:n.2812-81_2812-75del
NM_001458.4:c.2812-81_2812-75del , LRG_870t1:c.2812-81_2812-75del	NP_001449.3:n.2812-81_2812-75del
NM_001127487.2:c.2812-81_2812-75del	NP_001120959.1:n.2812-81_2812-75del
NM_001458.5:c.2812-81_2812-75del MANE Select	NP_001449.3:n.2812-81_2812-75del