Canonical Allele Identifier: CA457846230
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs779902112
MyVariant Identifiers: chr7:g.128477457T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837403T>C , CM000669.2:g.128837403T>C GRCh38
NC_000007.13:g.128477457T>C , CM000669.1:g.128477457T>C GRCh37
NC_000007.12:g.128264693T>C NCBI36
NG_011807.1:g.11975T>C , LRG_870:g.11975T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.705T>C MANE Select ENSP00000327145.8:p.Ile235=
ENST00000325888.12:c.705T>C ENSP00000327145.8:p.Ile235=
ENST00000346177.6:c.705T>C ENSP00000344002.6:p.Ile235=
NM_001127487.1:c.705T>C NP_001120959.1:p.Ile235=
NM_001458.4:c.705T>C , LRG_870t1:c.705T>C NP_001449.3:p.Ile235=
NM_001127487.2:c.705T>C NP_001120959.1:p.Ile235=
NM_001458.5:c.705T>C MANE Select NP_001449.3:p.Ile235=
Search 100 bp 5'
Search 100 bp 3'