Canonical Allele Identifier: CA2579014051

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841121_128841148del , CM000669.2:g.128841121_128841148del	GRCh38
NC_000007.13:g.128481175_128481202del , CM000669.1:g.128481175_128481202del	GRCh37
NC_000007.12:g.128268411_128268438del	NCBI36
NG_011807.1:g.15693_15720del , LRG_870:g.15693_15720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1814-49_1814-22del MANE Select	ENSP00000327145.8:n.1814-49_1814-22del
ENST00000325888.12:c.1814-49_1814-22del	ENSP00000327145.8:n.1814-49_1814-22del
ENST00000346177.6:c.1814-49_1814-22del	ENSP00000344002.6:n.1814-49_1814-22del
NM_001127487.1:c.1814-49_1814-22del	NP_001120959.1:n.1814-49_1814-22del
NM_001458.4:c.1814-49_1814-22del , LRG_870t1:c.1814-49_1814-22del	NP_001449.3:n.1814-49_1814-22del
NM_001127487.2:c.1814-49_1814-22del	NP_001120959.1:n.1814-49_1814-22del
NM_001458.5:c.1814-49_1814-22del MANE Select	NP_001449.3:n.1814-49_1814-22del