Canonical Allele Identifier: CA1742570728
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851362_128851366delinsTGAGG , CM000669.2:g.128851362_128851366delinsTGAGG GRCh38
NC_000007.13:g.128491416_128491420delinsTGAGG , CM000669.1:g.128491416_128491420delinsTGAGG GRCh37
NC_000007.12:g.128278652_128278656delinsTGAGG NCBI36
NG_011807.1:g.25934_25938delinsTGAGG , LRG_870:g.25934_25938delinsTGAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5668+2_5668+6delinsTGAGG (FLNC) MANE Select ENSP00000327145.8:n.5668+2_5668+6delinsTGAGG
ENST00000325888.12:c.5668+2_5668+6delinsTGAGG (FLNC) ENSP00000327145.8:n.5668+2_5668+6delinsTGAGG
ENST00000346177.6:c.5569+2_5569+6delinsTGAGG (FLNC) ENSP00000344002.6:n.5569+2_5569+6delinsTGAGG
NM_001127487.1:c.5569+2_5569+6delinsTGAGG (FLNC) NP_001120959.1:n.5569+2_5569+6delinsTGAGG
NM_001458.4:c.5668+2_5668+6delinsTGAGG , LRG_870t1:c.5668+2_5668+6delinsTGAGG (FLNC) NP_001449.3:n.5668+2_5668+6delinsTGAGG
NR_149055.1:n.315+35_315+39delinsCCTCA (FLNC-AS1)
NM_001127487.2:c.5569+2_5569+6delinsTGAGG (FLNC) NP_001120959.1:n.5569+2_5569+6delinsTGAGG
NM_001458.5:c.5668+2_5668+6delinsTGAGG (FLNC) MANE Select NP_001449.3:n.5668+2_5668+6delinsTGAGG
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