Canonical Allele Identifier: CA1742570762
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851371T= , CM000669.2:g.128851371T= GRCh38
NC_000007.13:g.128491425T= , CM000669.1:g.128491425T= GRCh37
NC_000007.12:g.128278661T= NCBI36
NG_011807.1:g.25943T= , LRG_870:g.25943T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5668+11T= (FLNC) MANE Select ENSP00000327145.8:n.5668+11T=
ENST00000325888.12:c.5668+11T= (FLNC) ENSP00000327145.8:n.5668+11T=
ENST00000346177.6:c.5569+11T= (FLNC) ENSP00000344002.6:n.5569+11T=
NM_001127487.1:c.5569+11T= (FLNC) NP_001120959.1:n.5569+11T=
NM_001458.4:c.5668+11T= , LRG_870t1:c.5668+11T= (FLNC) NP_001449.3:n.5668+11T=
NR_149055.1:n.315+30A= (FLNC-AS1)
NM_001127487.2:c.5569+11T= (FLNC) NP_001120959.1:n.5569+11T=
NM_001458.5:c.5668+11T= (FLNC) MANE Select NP_001449.3:n.5668+11T=
Search 100 bp 5'
Search 100 bp 3'