Canonical Allele Identifier: CA166212638
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs893378802

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835203A>T , CM000669.2:g.128835203A>T GRCh38
NC_000007.13:g.128475257A>T , CM000669.1:g.128475257A>T GRCh37
NC_000007.12:g.128262493A>T NCBI36
NG_011807.1:g.9775A>T , LRG_870:g.9775A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-123A>T MANE Select ENSP00000327145.8:n.353-123A>T
ENST00000325888.12:c.353-123A>T ENSP00000327145.8:n.353-123A>T
ENST00000346177.6:c.353-123A>T ENSP00000344002.6:n.353-123A>T
NM_001127487.1:c.353-123A>T NP_001120959.1:n.353-123A>T
NM_001458.4:c.353-123A>T , LRG_870t1:c.353-123A>T NP_001449.3:n.353-123A>T
NM_001127487.2:c.353-123A>T NP_001120959.1:n.353-123A>T
NM_001458.5:c.353-123A>T MANE Select NP_001449.3:n.353-123A>T