Canonical Allele Identifier: CA1742516881
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs4731518
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835061A>T , CM000669.2:g.128835061A>T GRCh38
NC_000007.13:g.128475115A>T , CM000669.1:g.128475115A>T GRCh37
NC_000007.12:g.128262351A>T NCBI36
NG_011807.1:g.9633A>T , LRG_870:g.9633A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-265A>T MANE Select ENSP00000327145.8:n.353-265A>T
ENST00000325888.12:c.353-265A>T ENSP00000327145.8:n.353-265A>T
ENST00000346177.6:c.353-265A>T ENSP00000344002.6:n.353-265A>T
NM_001127487.1:c.353-265A>T NP_001120959.1:n.353-265A>T
NM_001458.4:c.353-265A>T , LRG_870t1:c.353-265A>T NP_001449.3:n.353-265A>T
NM_001127487.2:c.353-265A>T NP_001120959.1:n.353-265A>T
NM_001458.5:c.353-265A>T MANE Select NP_001449.3:n.353-265A>T
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