Canonical Allele Identifier: CA1742569519
Gene: FLNC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841336C= , CM000669.2:g.128841336C= GRCh38
NC_000007.13:g.128481390C= , CM000669.1:g.128481390C= GRCh37
NC_000007.12:g.128268626C= NCBI36
NG_011807.1:g.15908C= , LRG_870:g.15908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1980C= MANE Select ENSP00000327145.8:p.Pro660=
ENST00000325888.12:c.1980C= ENSP00000327145.8:p.Pro660=
ENST00000346177.6:c.1980C= ENSP00000344002.6:p.Pro660=
ENST00000388853.3:n.6C=
NM_001127487.1:c.1980C= NP_001120959.1:p.Pro660=
NM_001458.4:c.1980C= , LRG_870t1:c.1980C= NP_001449.3:p.Pro660=
NM_001127487.2:c.1980C= NP_001120959.1:p.Pro660=
NM_001458.5:c.1980C= MANE Select NP_001449.3:p.Pro660=
Search 100 bp 5'
Search 100 bp 3'