Canonical Allele Identifier: CA1742563856
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849254G= , CM000669.2:g.128849254G= GRCh38
NC_000007.13:g.128489308G= , CM000669.1:g.128489308G= GRCh37
NC_000007.12:g.128276544G= NCBI36
NG_011807.1:g.23826G= , LRG_870:g.23826G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4951+50G= MANE Select ENSP00000327145.8:n.4951+50G=
ENST00000325888.12:c.4951+50G= ENSP00000327145.8:n.4951+50G=
ENST00000346177.6:c.4951+50G= ENSP00000344002.6:n.4951+50G=
NM_001127487.1:c.4951+50G= NP_001120959.1:n.4951+50G=
NM_001458.4:c.4951+50G= , LRG_870t1:c.4951+50G= NP_001449.3:n.4951+50G=
NM_001127487.2:c.4951+50G= NP_001120959.1:n.4951+50G=
NM_001458.5:c.4951+50G= MANE Select NP_001449.3:n.4951+50G=