Canonical Allele Identifier: CA1742585341
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128845193A= , CM000669.2:g.128845193A= GRCh38
NC_000007.13:g.128485247A= , CM000669.1:g.128485247A= GRCh37
NC_000007.12:g.128272483A= NCBI36
NG_011807.1:g.19765A= , LRG_870:g.19765A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3728A= MANE Select ENSP00000327145.8:p.His1243=
ENST00000325888.12:c.3728A= ENSP00000327145.8:p.His1243=
ENST00000346177.6:c.3728A= ENSP00000344002.6:p.His1243=
NM_001127487.1:c.3728A= NP_001120959.1:p.His1243=
NM_001458.4:c.3728A= , LRG_870t1:c.3728A= NP_001449.3:p.His1243=
NM_001127487.2:c.3728A= NP_001120959.1:p.His1243=
NM_001458.5:c.3728A= MANE Select NP_001449.3:p.His1243=