Canonical Allele Identifier: CA2579014137
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842765A>G , CM000669.2:g.128842765A>G GRCh38
NC_000007.13:g.128482819A>G , CM000669.1:g.128482819A>G GRCh37
NC_000007.12:g.128270055A>G NCBI36
NG_011807.1:g.17337A>G , LRG_870:g.17337A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2390-29A>G MANE Select ENSP00000327145.8:n.2390-29A>G
ENST00000325888.12:c.2390-29A>G ENSP00000327145.8:n.2390-29A>G
ENST00000346177.6:c.2390-29A>G ENSP00000344002.6:n.2390-29A>G
ENST00000388853.3:n.506-29A>G
NM_001127487.1:c.2390-29A>G NP_001120959.1:n.2390-29A>G
NM_001458.4:c.2390-29A>G , LRG_870t1:c.2390-29A>G NP_001449.3:n.2390-29A>G
NM_001127487.2:c.2390-29A>G NP_001120959.1:n.2390-29A>G
NM_001458.5:c.2390-29A>G MANE Select NP_001449.3:n.2390-29A>G