Canonical Allele Identifier: CA1742571190
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851499A= , CM000669.2:g.128851499A= GRCh38
NC_000007.13:g.128491553A= , CM000669.1:g.128491553A= GRCh37
NC_000007.12:g.128278789A= NCBI36
NG_011807.1:g.26071A= , LRG_870:g.26071A=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5713A= (FLNC) MANE Select ENSP00000327145.8:p.Thr1905=
ENST00000325888.12:c.5713A= (FLNC) ENSP00000327145.8:p.Thr1905=
ENST00000346177.6:c.5614A= (FLNC) ENSP00000344002.6:p.Thr1872=
NM_001127487.1:c.5614A= (FLNC) NP_001120959.1:p.Thr1872=
NM_001458.4:c.5713A= , LRG_870t1:c.5713A= (FLNC) NP_001449.3:p.Thr1905=
NR_149055.1:n.217T= (FLNC-AS1)
NM_001127487.2:c.5614A= (FLNC) NP_001120959.1:p.Thr1872=
NM_001458.5:c.5713A= (FLNC) MANE Select NP_001449.3:p.Thr1905=
Search 100 bp 5'
Search 100 bp 3'