Canonical Allele Identifier: CA578151189

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1362449241
• gnomAD v2: 7-128498690-T-C
• gnomAD v3: 7-128858636-T-C
• gnomAD v4: 7-128858636-T-C
• MyVariant Identifiers: chr7:g.128498690T>C (hg19) ; chr7:g.128858636T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858636T>C , CM000669.2:g.128858636T>C	GRCh38
NC_000007.13:g.128498690T>C , CM000669.1:g.128498690T>C	GRCh37
NC_000007.12:g.128285926T>C	NCBI36
NG_011807.1:g.33208T>C , LRG_870:g.33208T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*113T>C (FLNC) MANE Select	ENSP00000327145.8:n.*113T>C
ENST00000325888.12:c.*113T>C (FLNC)	ENSP00000327145.8:n.*113T>C
ENST00000346177.6:c.*113T>C (FLNC)	ENSP00000344002.6:n.*113T>C
NM_001127487.1:c.*113T>C (FLNC)	NP_001120959.1:n.*113T>C
NM_001458.4:c.*113T>C , LRG_870t1:c.*113T>C (FLNC)	NP_001449.3:n.*113T>C
NR_149055.1:n.102+3889A>G (FLNC-AS1)
NM_001127487.2:c.*113T>C (FLNC)	NP_001120959.1:n.*113T>C
NM_001458.5:c.*113T>C (FLNC) MANE Select	NP_001449.3:n.*113T>C