Canonical Allele Identifier: CA2715892036
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs2128934405

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128838337_128838370del , CM000669.2:g.128838337_128838370del GRCh38
NC_000007.13:g.128478391_128478424del , CM000669.1:g.128478391_128478424del GRCh37
NC_000007.12:g.128265627_128265660del NCBI36
NG_011807.1:g.12909_12942del , LRG_870:g.12909_12942del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1118_1151del MANE Select ENSP00000327145.8:p.Gly373AlafsTer30
ENST00000325888.12:c.1118_1151del ENSP00000327145.8:p.Gly373AlafsTer30
ENST00000346177.6:c.1118_1151del ENSP00000344002.6:p.Gly373AlafsTer30
NM_001127487.1:c.1118_1151del NP_001120959.1:p.Gly373AlafsTer30
NM_001458.4:c.1118_1151del , LRG_870t1:c.1118_1151del NP_001449.3:p.Gly373AlafsTer30
NM_001127487.2:c.1118_1151del NP_001120959.1:p.Gly373AlafsTer30
NM_001458.5:c.1118_1151del MANE Select NP_001449.3:p.Gly373AlafsTer30