Canonical Allele Identifier: CA1742567045
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841043C= , CM000669.2:g.128841043C= GRCh38
NC_000007.13:g.128481097C= , CM000669.1:g.128481097C= GRCh37
NC_000007.12:g.128268333C= NCBI36
NG_011807.1:g.15615C= , LRG_870:g.15615C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1813+73C= MANE Select ENSP00000327145.8:n.1813+73C=
ENST00000325888.12:c.1813+73C= ENSP00000327145.8:n.1813+73C=
ENST00000346177.6:c.1813+73C= ENSP00000344002.6:n.1813+73C=
NM_001127487.1:c.1813+73C= NP_001120959.1:n.1813+73C=
NM_001458.4:c.1813+73C= , LRG_870t1:c.1813+73C= NP_001449.3:n.1813+73C=
NM_001127487.2:c.1813+73C= NP_001120959.1:n.1813+73C=
NM_001458.5:c.1813+73C= MANE Select NP_001449.3:n.1813+73C=