Canonical Allele Identifier: CA369204003
Gene: FLNC HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128489453G>T (hg19) chr7:g.128849399G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849399G>T , CM000669.2:g.128849399G>T GRCh38
NC_000007.13:g.128489453G>T , CM000669.1:g.128489453G>T GRCh37
NC_000007.12:g.128276689G>T NCBI36
NG_011807.1:g.23971G>T , LRG_870:g.23971G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5020G>T MANE Select ENSP00000327145.8:p.Gly1674Cys
ENST00000325888.12:c.5020G>T ENSP00000327145.8:p.Gly1674Cys
ENST00000346177.6:c.5020G>T ENSP00000344002.6:p.Gly1674Cys
NM_001127487.1:c.5020G>T NP_001120959.1:p.Gly1674Cys
NM_001458.4:c.5020G>T , LRG_870t1:c.5020G>T NP_001449.3:p.Gly1674Cys
NM_001127487.2:c.5020G>T NP_001120959.1:p.Gly1674Cys
NM_001458.5:c.5020G>T MANE Select NP_001449.3:p.Gly1674Cys
Search 100 bp 5'
Search 100 bp 3'