Canonical Allele Identifier: CA166176333

Gene: FLNC

Linked Data

• dbSNP Id: rs35282227
• MyVariant Identifiers: chr7:g.128483411_128483412insG (hg19) ; chr7:g.128843357_128843358insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843361dup , CM000669.2:g.128843361dup	GRCh38
NC_000007.13:g.128483415dup , CM000669.1:g.128483415dup	GRCh37
NC_000007.12:g.128270651dup	NCBI36
NG_011807.1:g.17933dup , LRG_870:g.17933dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2641+42dup MANE Select	ENSP00000327145.8:n.2641+42dup
ENST00000325888.12:c.2641+42dup	ENSP00000327145.8:n.2641+42dup
ENST00000346177.6:c.2641+42dup	ENSP00000344002.6:n.2641+42dup
NM_001127487.1:c.2641+42dup	NP_001120959.1:n.2641+42dup
NM_001458.4:c.2641+42dup , LRG_870t1:c.2641+42dup	NP_001449.3:n.2641+42dup
NM_001127487.2:c.2641+42dup	NP_001120959.1:n.2641+42dup
NM_001458.5:c.2641+42dup MANE Select	NP_001449.3:n.2641+42dup