Canonical Allele Identifier: CA1742545935
Gene: FLNC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840124G= , CM000669.2:g.128840124G= GRCh38
NC_000007.13:g.128480178G= , CM000669.1:g.128480178G= GRCh37
NC_000007.12:g.128267414G= NCBI36
NG_011807.1:g.14696G= , LRG_870:g.14696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1513G= MANE Select ENSP00000327145.8:p.Gly505=
ENST00000325888.12:c.1513G= ENSP00000327145.8:p.Gly505=
ENST00000346177.6:c.1513G= ENSP00000344002.6:p.Gly505=
NM_001127487.1:c.1513G= NP_001120959.1:p.Gly505=
NM_001458.4:c.1513G= , LRG_870t1:c.1513G= NP_001449.3:p.Gly505=
NM_001127487.2:c.1513G= NP_001120959.1:p.Gly505=
NM_001458.5:c.1513G= MANE Select NP_001449.3:p.Gly505=
Search 100 bp 5'
Search 100 bp 3'