Canonical Allele Identifier: CA2684819248
Gene: FLNC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835212C>A , CM000669.2:g.128835212C>A GRCh38
NC_000007.13:g.128475266C>A , CM000669.1:g.128475266C>A GRCh37
NC_000007.12:g.128262502C>A NCBI36
NG_011807.1:g.9784C>A , LRG_870:g.9784C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-114C>A MANE Select ENSP00000327145.8:n.353-114C>A
ENST00000325888.12:c.353-114C>A ENSP00000327145.8:n.353-114C>A
ENST00000346177.6:c.353-114C>A ENSP00000344002.6:n.353-114C>A
NM_001127487.1:c.353-114C>A NP_001120959.1:n.353-114C>A
NM_001458.4:c.353-114C>A , LRG_870t1:c.353-114C>A NP_001449.3:n.353-114C>A
NM_001127487.2:c.353-114C>A NP_001120959.1:n.353-114C>A
NM_001458.5:c.353-114C>A MANE Select NP_001449.3:n.353-114C>A