Canonical Allele Identifier: CA4475044

Gene: FLNC

Linked Data

• dbSNP Id: rs762164440
• ExAC: 7:128484970 C / CACTACGGGTGAAACCCAAAGAGTTCAGCCA
• MyVariant Identifiers: chr7:g.128484970_128484971insACTACGGGTGAAACCCAAAGAGTTCAGCCA (hg19) ; chr7:g.128844916_128844917insACTACGGGTGAAACCCAAAGAGTTCAGCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128844916_128844917insACTACGGGTGAAACCCAAAGAGTTCAGCCA , CM000669.2:g.128844916_128844917insACTACGGGTGAAACCCAAAGAGTTCAGCCA	GRCh38
NC_000007.13:g.128484970_128484971insACTACGGGTGAAACCCAAAGAGTTCAGCCA , CM000669.1:g.128484970_128484971insACTACGGGTGAAACCCAAAGAGTTCAGCCA	GRCh37
NC_000007.12:g.128272206_128272207insACTACGGGTGAAACCCAAAGAGTTCAGCCA	NCBI36
NG_011807.1:g.19488_19489insACTACGGGTGAAACCCAAAGAGTTCAGCCA , LRG_870:g.19488_19489insACTACGGGTGAAACCCAAAGAGTTCAGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA MANE Select	ENSP00000327145.8:p.Pro1151HisfsTer4
ENST00000325888.12:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA	ENSP00000327145.8:p.Pro1151HisfsTer4
ENST00000346177.6:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA	ENSP00000344002.6:p.Pro1151HisfsTer4
NM_001127487.1:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA	NP_001120959.1:p.Pro1151HisfsTer4
NM_001458.4:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA , LRG_870t1:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA	NP_001449.3:p.Pro1151HisfsTer4
NM_001127487.2:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA	NP_001120959.1:p.Pro1151HisfsTer4
NM_001458.5:c.3451_3452insACTACGGGTGAAACCCAAAGAGTTCAGCCA MANE Select	NP_001449.3:p.Pro1151HisfsTer4