Canonical Allele Identifier: CA2684818330
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128844860-A-AAC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844860_128844861insAC , CM000669.2:g.128844860_128844861insAC GRCh38
NC_000007.13:g.128484914_128484915insAC , CM000669.1:g.128484914_128484915insAC GRCh37
NC_000007.12:g.128272150_128272151insAC NCBI36
NG_011807.1:g.19432_19433insAC , LRG_870:g.19432_19433insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3395_3396insAC MANE Select ENSP00000327145.8:p.Asn1132LysfsTer?
ENST00000325888.12:c.3395_3396insAC ENSP00000327145.8:p.Asn1132LysfsTer?
ENST00000346177.6:c.3395_3396insAC ENSP00000344002.6:p.Asn1132LysfsTer?
NM_001127487.1:c.3395_3396insAC NP_001120959.1:p.Asn1132LysfsTer?
NM_001458.4:c.3395_3396insAC , LRG_870t1:c.3395_3396insAC NP_001449.3:p.Asn1132LysfsTer?
NM_001127487.2:c.3395_3396insAC NP_001120959.1:p.Asn1132LysfsTer?
NM_001458.5:c.3395_3396insAC MANE Select NP_001449.3:p.Asn1132LysfsTer?
Search 100 bp 5'
Search 100 bp 3'