Canonical Allele Identifier: CA1742566560
Gene: FLNC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840994A= , CM000669.2:g.128840994A= GRCh38
NC_000007.13:g.128481048A= , CM000669.1:g.128481048A= GRCh37
NC_000007.12:g.128268284A= NCBI36
NG_011807.1:g.15566A= , LRG_870:g.15566A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1813+24A= MANE Select ENSP00000327145.8:n.1813+24A=
ENST00000325888.12:c.1813+24A= ENSP00000327145.8:n.1813+24A=
ENST00000346177.6:c.1813+24A= ENSP00000344002.6:n.1813+24A=
NM_001127487.1:c.1813+24A= NP_001120959.1:n.1813+24A=
NM_001458.4:c.1813+24A= , LRG_870t1:c.1813+24A= NP_001449.3:n.1813+24A=
NM_001127487.2:c.1813+24A= NP_001120959.1:n.1813+24A=
NM_001458.5:c.1813+24A= MANE Select NP_001449.3:n.1813+24A=
Search 100 bp 5'
Search 100 bp 3'