Canonical Allele Identifier: CA2684812391
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128851385-T-TGGGGTGGAGACTCACCAGGGGCA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851392_128851414dup , CM000669.2:g.128851392_128851414dup GRCh38
NC_000007.13:g.128491446_128491468dup , CM000669.1:g.128491446_128491468dup GRCh37
NC_000007.12:g.128278682_128278704dup NCBI36
NG_011807.1:g.25964_25986dup , LRG_870:g.25964_25986dup

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5668+32_5669-41dup (FLNC) MANE Select ENSP00000327145.8:n.5668+32_5669-41dup
ENST00000325888.12:c.5668+32_5669-41dup (FLNC) ENSP00000327145.8:n.5668+32_5669-41dup
ENST00000346177.6:c.5569+32_5570-41dup (FLNC) ENSP00000344002.6:n.5569+32_5570-41dup
NM_001127487.1:c.5569+32_5570-41dup (FLNC) NP_001120959.1:n.5569+32_5570-41dup
NM_001458.4:c.5668+32_5669-41dup , LRG_870t1:c.5668+32_5669-41dup (FLNC) NP_001449.3:n.5668+32_5669-41dup
NR_149055.1:n.308_315+15dup (FLNC-AS1)
NM_001127487.2:c.5569+32_5570-41dup (FLNC) NP_001120959.1:n.5569+32_5570-41dup
NM_001458.5:c.5668+32_5669-41dup (FLNC) MANE Select NP_001449.3:n.5668+32_5669-41dup
Search 100 bp 5'
Search 100 bp 3'