Canonical Allele Identifier: CA2684815675

Gene: FLNC

Linked Data

• gnomAD v4: 7-128849116-A-ACCCCCCCCCCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849121_128849122insCCCCCAAGCCCCC , CM000669.2:g.128849121_128849122insCCCCCAAGCCCCC	GRCh38
NC_000007.13:g.128489175_128489176insCCCCCAAGCCCCC , CM000669.1:g.128489175_128489176insCCCCCAAGCCCCC	GRCh37
NC_000007.12:g.128276411_128276412insCCCCCAAGCCCCC	NCBI36
NG_011807.1:g.23693_23694insCCCCCAAGCCCCC , LRG_870:g.23693_23694insCCCCCAAGCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-60_4928-59insCCCCCAAGCCCCC MANE Select	ENSP00000327145.8:n.4928-60_4928-59insCCCCCAAGCCCCC
ENST00000325888.12:c.4928-60_4928-59insCCCCCAAGCCCCC	ENSP00000327145.8:n.4928-60_4928-59insCCCCCAAGCCCCC
ENST00000346177.6:c.4928-60_4928-59insCCCCCAAGCCCCC	ENSP00000344002.6:n.4928-60_4928-59insCCCCCAAGCCCCC
NM_001127487.1:c.4928-60_4928-59insCCCCCAAGCCCCC	NP_001120959.1:n.4928-60_4928-59insCCCCCAAGCCCCC
NM_001458.4:c.4928-60_4928-59insCCCCCAAGCCCCC , LRG_870t1:c.4928-60_4928-59insCCCCCAAGCCCCC	NP_001449.3:n.4928-60_4928-59insCCCCCAAGCCCCC
NM_001127487.2:c.4928-60_4928-59insCCCCCAAGCCCCC	NP_001120959.1:n.4928-60_4928-59insCCCCCAAGCCCCC
NM_001458.5:c.4928-60_4928-59insCCCCCAAGCCCCC MANE Select	NP_001449.3:n.4928-60_4928-59insCCCCCAAGCCCCC