Canonical Allele Identifier: CA2579014531
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851388G>A , CM000669.2:g.128851388G>A GRCh38
NC_000007.13:g.128491442G>A , CM000669.1:g.128491442G>A GRCh37
NC_000007.12:g.128278678G>A NCBI36
NG_011807.1:g.25960G>A , LRG_870:g.25960G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5668+28G>A (FLNC) MANE Select ENSP00000327145.8:n.5668+28G>A
ENST00000325888.12:c.5668+28G>A (FLNC) ENSP00000327145.8:n.5668+28G>A
ENST00000346177.6:c.5569+28G>A (FLNC) ENSP00000344002.6:n.5569+28G>A
NM_001127487.1:c.5569+28G>A (FLNC) NP_001120959.1:n.5569+28G>A
NM_001458.4:c.5668+28G>A , LRG_870t1:c.5668+28G>A (FLNC) NP_001449.3:n.5668+28G>A
NR_149055.1:n.315+13C>T (FLNC-AS1)
NM_001127487.2:c.5569+28G>A (FLNC) NP_001120959.1:n.5569+28G>A
NM_001458.5:c.5668+28G>A (FLNC) MANE Select NP_001449.3:n.5668+28G>A