Canonical Allele Identifier: CA1742579628
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843218T= , CM000669.2:g.128843218T= GRCh38
NC_000007.13:g.128483272T= , CM000669.1:g.128483272T= GRCh37
NC_000007.12:g.128270508T= NCBI36
NG_011807.1:g.17790T= , LRG_870:g.17790T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2551-11T= MANE Select ENSP00000327145.8:n.2551-11T=
ENST00000325888.12:c.2551-11T= ENSP00000327145.8:n.2551-11T=
ENST00000346177.6:c.2551-11T= ENSP00000344002.6:n.2551-11T=
NM_001127487.1:c.2551-11T= NP_001120959.1:n.2551-11T=
NM_001458.4:c.2551-11T= , LRG_870t1:c.2551-11T= NP_001449.3:n.2551-11T=
NM_001127487.2:c.2551-11T= NP_001120959.1:n.2551-11T=
NM_001458.5:c.2551-11T= MANE Select NP_001449.3:n.2551-11T=