Canonical Allele Identifier: CA1742584250
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844858C= , CM000669.2:g.128844858C= GRCh38
NC_000007.13:g.128484912C= , CM000669.1:g.128484912C= GRCh37
NC_000007.12:g.128272148C= NCBI36
NG_011807.1:g.19430C= , LRG_870:g.19430C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3393C= MANE Select ENSP00000327145.8:p.Ile1131=
ENST00000325888.12:c.3393C= ENSP00000327145.8:p.Ile1131=
ENST00000346177.6:c.3393C= ENSP00000344002.6:p.Ile1131=
NM_001127487.1:c.3393C= NP_001120959.1:p.Ile1131=
NM_001458.4:c.3393C= , LRG_870t1:c.3393C= NP_001449.3:p.Ile1131=
NM_001127487.2:c.3393C= NP_001120959.1:p.Ile1131=
NM_001458.5:c.3393C= MANE Select NP_001449.3:p.Ile1131=