Canonical Allele Identifier: CA4475340
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs533901277
ExAC: 7:128487951 T / TG
gnomAD v2: 7-128487951-T-TG
gnomAD v3: 7-128847897-T-TG
gnomAD v4: 7-128847897-T-TG
MyVariant Identifiers: chr7:g.128487951_128487952insG (hg19) chr7:g.128847897_128847898insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847901dup , CM000669.2:g.128847901dup GRCh38
NC_000007.13:g.128487955dup , CM000669.1:g.128487955dup GRCh37
NC_000007.12:g.128275191dup NCBI36
NG_011807.1:g.22473dup , LRG_870:g.22473dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4456+37dup MANE Select ENSP00000327145.8:n.4456+37dup
ENST00000325888.12:c.4456+37dup ENSP00000327145.8:n.4456+37dup
ENST00000346177.6:c.4456+37dup ENSP00000344002.6:n.4456+37dup
NM_001127487.1:c.4456+37dup NP_001120959.1:n.4456+37dup
NM_001458.4:c.4456+37dup , LRG_870t1:c.4456+37dup NP_001449.3:n.4456+37dup
NM_001127487.2:c.4456+37dup NP_001120959.1:n.4456+37dup
NM_001458.5:c.4456+37dup MANE Select NP_001449.3:n.4456+37dup
Search 100 bp 5'
Search 100 bp 3'