Canonical Allele Identifier: CA369192855
Gene: FLNC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843438C>G , CM000669.2:g.128843438C>G GRCh38
NC_000007.13:g.128483492C>G , CM000669.1:g.128483492C>G GRCh37
NC_000007.12:g.128270728C>G NCBI36
NG_011807.1:g.18010C>G , LRG_870:g.18010C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2672C>G MANE Select ENSP00000327145.8:p.Thr891Arg
ENST00000325888.12:c.2672C>G ENSP00000327145.8:p.Thr891Arg
ENST00000346177.6:c.2672C>G ENSP00000344002.6:p.Thr891Arg
NM_001127487.1:c.2672C>G NP_001120959.1:p.Thr891Arg
NM_001458.4:c.2672C>G , LRG_870t1:c.2672C>G NP_001449.3:p.Thr891Arg
NM_001127487.2:c.2672C>G NP_001120959.1:p.Thr891Arg
NM_001458.5:c.2672C>G MANE Select NP_001449.3:p.Thr891Arg