Canonical Allele Identifier: CA2684820186

Gene: FLNC

Linked Data

• gnomAD v4: 7-128839971-AGTGGTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128839972_128839977del , CM000669.2:g.128839972_128839977del	GRCh38
NC_000007.13:g.128480026_128480031del , CM000669.1:g.128480026_128480031del	GRCh37
NC_000007.12:g.128267262_128267267del	NCBI36
NG_011807.1:g.14544_14549del , LRG_870:g.14544_14549del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1412-51_1412-46del MANE Select	ENSP00000327145.8:n.1412-51_1412-46del
ENST00000325888.12:c.1412-51_1412-46del	ENSP00000327145.8:n.1412-51_1412-46del
ENST00000346177.6:c.1412-51_1412-46del	ENSP00000344002.6:n.1412-51_1412-46del
NM_001127487.1:c.1412-51_1412-46del	NP_001120959.1:n.1412-51_1412-46del
NM_001458.4:c.1412-51_1412-46del , LRG_870t1:c.1412-51_1412-46del	NP_001449.3:n.1412-51_1412-46del
NM_001127487.2:c.1412-51_1412-46del	NP_001120959.1:n.1412-51_1412-46del
NM_001458.5:c.1412-51_1412-46del MANE Select	NP_001449.3:n.1412-51_1412-46del