Canonical Allele Identifier: CA1742549789
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857070G= , CM000669.2:g.128857070G= GRCh38
NC_000007.13:g.128497124G= , CM000669.1:g.128497124G= GRCh37
NC_000007.12:g.128284360G= NCBI36
NG_011807.1:g.31642G= , LRG_870:g.31642G=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7562-48G= (FLNC) MANE Select ENSP00000327145.8:n.7562-48G=
ENST00000325888.12:c.7562-48G= (FLNC) ENSP00000327145.8:n.7562-48G=
ENST00000346177.6:c.7463-48G= (FLNC) ENSP00000344002.6:n.7463-48G=
NM_001127487.1:c.7463-48G= (FLNC) NP_001120959.1:n.7463-48G=
NM_001458.4:c.7562-48G= , LRG_870t1:c.7562-48G= (FLNC) NP_001449.3:n.7562-48G=
NR_149055.1:n.103-3673C= (FLNC-AS1)
NM_001127487.2:c.7463-48G= (FLNC) NP_001120959.1:n.7463-48G=
NM_001458.5:c.7562-48G= (FLNC) MANE Select NP_001449.3:n.7562-48G=
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