Canonical Allele Identifier: CA833136032

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1399013649
• MyVariant Identifiers: chr7:g.128497492_128497502del (hg19) ; chr7:g.128857438_128857448del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857439_128857449del , CM000669.2:g.128857439_128857449del	GRCh38
NC_000007.13:g.128497493_128497503del , CM000669.1:g.128497493_128497503del	GRCh37
NC_000007.12:g.128284729_128284739del	NCBI36
NG_011807.1:g.32011_32021del , LRG_870:g.32011_32021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+103_7780+113del (FLNC) MANE Select	ENSP00000327145.8:n.7780+103_7780+113del
ENST00000325888.12:c.7780+103_7780+113del (FLNC)	ENSP00000327145.8:n.7780+103_7780+113del
ENST00000346177.6:c.7681+103_7681+113del (FLNC)	ENSP00000344002.6:n.7681+103_7681+113del
NM_001127487.1:c.7681+103_7681+113del (FLNC)	NP_001120959.1:n.7681+103_7681+113del
NM_001458.4:c.7780+103_7780+113del , LRG_870t1:c.7780+103_7780+113del (FLNC)	NP_001449.3:n.7780+103_7780+113del
NR_149055.1:n.103-4051_103-4041del (FLNC-AS1)
NM_001127487.2:c.7681+103_7681+113del (FLNC)	NP_001120959.1:n.7681+103_7681+113del
NM_001458.5:c.7780+103_7780+113del (FLNC) MANE Select	NP_001449.3:n.7780+103_7780+113del