Canonical Allele Identifier: CA1107055075
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809061482

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856451G>A , CM000669.2:g.128856451G>A GRCh38
NC_000007.13:g.128496505G>A , CM000669.1:g.128496505G>A GRCh37
NC_000007.12:g.128283741G>A NCBI36
NG_011807.1:g.31023G>A , LRG_870:g.31023G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7252-67G>A (FLNC) MANE Select ENSP00000327145.8:n.7252-67G>A
ENST00000325888.12:c.7252-67G>A (FLNC) ENSP00000327145.8:n.7252-67G>A
ENST00000346177.6:c.7153-67G>A (FLNC) ENSP00000344002.6:n.7153-67G>A
NM_001127487.1:c.7153-67G>A (FLNC) NP_001120959.1:n.7153-67G>A
NM_001458.4:c.7252-67G>A , LRG_870t1:c.7252-67G>A (FLNC) NP_001449.3:n.7252-67G>A
NR_149055.1:n.103-3054C>T (FLNC-AS1)
NM_001127487.2:c.7153-67G>A (FLNC) NP_001120959.1:n.7153-67G>A
NM_001458.5:c.7252-67G>A (FLNC) MANE Select NP_001449.3:n.7252-67G>A