Canonical Allele Identifier: CA1107055651
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1808703779

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849258_128849279dup , CM000669.2:g.128849258_128849279dup GRCh38
NC_000007.13:g.128489312_128489333dup , CM000669.1:g.128489312_128489333dup GRCh37
NC_000007.12:g.128276548_128276569dup NCBI36
NG_011807.1:g.23830_23851dup , LRG_870:g.23830_23851dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4951+54_4952-52dup MANE Select ENSP00000327145.8:n.4951+54_4952-52dup
ENST00000325888.12:c.4951+54_4952-52dup ENSP00000327145.8:n.4951+54_4952-52dup
ENST00000346177.6:c.4951+54_4952-52dup ENSP00000344002.6:n.4951+54_4952-52dup
NM_001127487.1:c.4951+54_4952-52dup NP_001120959.1:n.4951+54_4952-52dup
NM_001458.4:c.4951+54_4952-52dup , LRG_870t1:c.4951+54_4952-52dup NP_001449.3:n.4951+54_4952-52dup
NM_001127487.2:c.4951+54_4952-52dup NP_001120959.1:n.4951+54_4952-52dup
NM_001458.5:c.4951+54_4952-52dup MANE Select NP_001449.3:n.4951+54_4952-52dup