Canonical Allele Identifier: CA1742588474
Gene: FLNC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128846790G= , CM000669.2:g.128846790G= GRCh38
NC_000007.13:g.128486844G= , CM000669.1:g.128486844G= GRCh37
NC_000007.12:g.128274080G= NCBI36
NG_011807.1:g.21362G= , LRG_870:g.21362G=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4173G= MANE Select ENSP00000327145.8:p.Ser1391=
ENST00000325888.12:c.4173G= ENSP00000327145.8:p.Ser1391=
ENST00000346177.6:c.4173G= ENSP00000344002.6:p.Ser1391=
NM_001127487.1:c.4173G= NP_001120959.1:p.Ser1391=
NM_001458.4:c.4173G= , LRG_870t1:c.4173G= NP_001449.3:p.Ser1391=
NM_001127487.2:c.4173G= NP_001120959.1:p.Ser1391=
NM_001458.5:c.4173G= MANE Select NP_001449.3:p.Ser1391=
Search 100 bp 5'
Search 100 bp 3'