Canonical Allele Identifier: CA369200492
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1229921536
MyVariant Identifiers: chr7:g.128486842T>C (hg19) chr7:g.128846788T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128846788T>C , CM000669.2:g.128846788T>C GRCh38
NC_000007.13:g.128486842T>C , CM000669.1:g.128486842T>C GRCh37
NC_000007.12:g.128274078T>C NCBI36
NG_011807.1:g.21360T>C , LRG_870:g.21360T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4171T>C MANE Select ENSP00000327145.8:p.Ser1391Pro
ENST00000325888.12:c.4171T>C ENSP00000327145.8:p.Ser1391Pro
ENST00000346177.6:c.4171T>C ENSP00000344002.6:p.Ser1391Pro
NM_001127487.1:c.4171T>C NP_001120959.1:p.Ser1391Pro
NM_001458.4:c.4171T>C , LRG_870t1:c.4171T>C NP_001449.3:p.Ser1391Pro
NM_001127487.2:c.4171T>C NP_001120959.1:p.Ser1391Pro
NM_001458.5:c.4171T>C MANE Select NP_001449.3:p.Ser1391Pro
Search 100 bp 5'
Search 100 bp 3'