Canonical Allele Identifier: CA918127264

Gene: FLNC

Linked Data

• dbSNP Id: rs1585158504

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843362_128843364del , CM000669.2:g.128843362_128843364del	GRCh38
NC_000007.13:g.128483416_128483418del , CM000669.1:g.128483416_128483418del	GRCh37
NC_000007.12:g.128270652_128270654del	NCBI36
NG_011807.1:g.17934_17936del , LRG_870:g.17934_17936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2641+43_2642-44del MANE Select	ENSP00000327145.8:n.2641+43_2642-44del
ENST00000325888.12:c.2641+43_2642-44del	ENSP00000327145.8:n.2641+43_2642-44del
ENST00000346177.6:c.2641+43_2642-44del	ENSP00000344002.6:n.2641+43_2642-44del
NM_001127487.1:c.2641+43_2642-44del	NP_001120959.1:n.2641+43_2642-44del
NM_001458.4:c.2641+43_2642-44del , LRG_870t1:c.2641+43_2642-44del	NP_001449.3:n.2641+43_2642-44del
NM_001127487.2:c.2641+43_2642-44del	NP_001120959.1:n.2641+43_2642-44del
NM_001458.5:c.2641+43_2642-44del MANE Select	NP_001449.3:n.2641+43_2642-44del