Canonical Allele Identifier: CA1742551738
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858162G= , CM000669.2:g.128858162G= GRCh38
NC_000007.13:g.128498216G= , CM000669.1:g.128498216G= GRCh37
NC_000007.12:g.128285452G= NCBI36
NG_011807.1:g.32734G= , LRG_870:g.32734G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7935G= (FLNC) MANE Select ENSP00000327145.8:p.Leu2645=
ENST00000325888.12:c.7935G= (FLNC) ENSP00000327145.8:p.Leu2645=
ENST00000346177.6:c.7836G= (FLNC) ENSP00000344002.6:p.Leu2612=
NM_001127487.1:c.7836G= (FLNC) NP_001120959.1:p.Leu2612=
NM_001458.4:c.7935G= , LRG_870t1:c.7935G= (FLNC) NP_001449.3:p.Leu2645=
NR_149055.1:n.102+4363C= (FLNC-AS1)
NM_001127487.2:c.7836G= (FLNC) NP_001120959.1:p.Leu2612=
NM_001458.5:c.7935G= (FLNC) MANE Select NP_001449.3:p.Leu2645=
Search 100 bp 5'
Search 100 bp 3'