Canonical Allele Identifier: CA2684815744

Gene: FLNC

Linked Data

• gnomAD v4: 7-128849139-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849139A>C , CM000669.2:g.128849139A>C	GRCh38
NC_000007.13:g.128489193A>C , CM000669.1:g.128489193A>C	GRCh37
NC_000007.12:g.128276429A>C	NCBI36
NG_011807.1:g.23711A>C , LRG_870:g.23711A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-42A>C MANE Select	ENSP00000327145.8:n.4928-42A>C
ENST00000325888.12:c.4928-42A>C	ENSP00000327145.8:n.4928-42A>C
ENST00000346177.6:c.4928-42A>C	ENSP00000344002.6:n.4928-42A>C
NM_001127487.1:c.4928-42A>C	NP_001120959.1:n.4928-42A>C
NM_001458.4:c.4928-42A>C , LRG_870t1:c.4928-42A>C	NP_001449.3:n.4928-42A>C
NM_001127487.2:c.4928-42A>C	NP_001120959.1:n.4928-42A>C
NM_001458.5:c.4928-42A>C MANE Select	NP_001449.3:n.4928-42A>C