Canonical Allele Identifier: CA1742568668
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841198C= , CM000669.2:g.128841198C= GRCh38
NC_000007.13:g.128481252C= , CM000669.1:g.128481252C= GRCh37
NC_000007.12:g.128268488C= NCBI36
NG_011807.1:g.15770C= , LRG_870:g.15770C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1842C= MANE Select ENSP00000327145.8:p.Ala614=
ENST00000325888.12:c.1842C= ENSP00000327145.8:p.Ala614=
ENST00000346177.6:c.1842C= ENSP00000344002.6:p.Ala614=
NM_001127487.1:c.1842C= NP_001120959.1:p.Ala614=
NM_001458.4:c.1842C= , LRG_870t1:c.1842C= NP_001449.3:p.Ala614=
NM_001127487.2:c.1842C= NP_001120959.1:p.Ala614=
NM_001458.5:c.1842C= MANE Select NP_001449.3:p.Ala614=