Canonical Allele Identifier: CA578150114

Gene: FLNC

Linked Data

• dbSNP Id: rs753342024
• gnomAD v2: 7-128477670-G-C
• gnomAD v4: 7-128837616-G-C
• MyVariant Identifiers: chr7:g.128477670G>C (hg19) ; chr7:g.128837616G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837616G>C , CM000669.2:g.128837616G>C	GRCh38
NC_000007.13:g.128477670G>C , CM000669.1:g.128477670G>C	GRCh37
NC_000007.12:g.128264906G>C	NCBI36
NG_011807.1:g.12188G>C , LRG_870:g.12188G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.851-21G>C MANE Select	ENSP00000327145.8:n.851-21G>C
ENST00000325888.12:c.851-21G>C	ENSP00000327145.8:n.851-21G>C
ENST00000346177.6:c.851-21G>C	ENSP00000344002.6:n.851-21G>C
NM_001127487.1:c.851-21G>C	NP_001120959.1:n.851-21G>C
NM_001458.4:c.851-21G>C , LRG_870t1:c.851-21G>C	NP_001449.3:n.851-21G>C
NM_001127487.2:c.851-21G>C	NP_001120959.1:n.851-21G>C
NM_001458.5:c.851-21G>C MANE Select	NP_001449.3:n.851-21G>C