Canonical Allele Identifier: CA166196831

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs997465232
• gnomAD v4: 7-128858650-T-C
• MyVariant Identifiers: chr7:g.128498704T>C (hg19) ; chr7:g.128858650T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858650T>C , CM000669.2:g.128858650T>C	GRCh38
NC_000007.13:g.128498704T>C , CM000669.1:g.128498704T>C	GRCh37
NC_000007.12:g.128285940T>C	NCBI36
NG_011807.1:g.33222T>C , LRG_870:g.33222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*127T>C (FLNC) MANE Select	ENSP00000327145.8:n.*127T>C
ENST00000325888.12:c.*127T>C (FLNC)	ENSP00000327145.8:n.*127T>C
ENST00000346177.6:c.*127T>C (FLNC)	ENSP00000344002.6:n.*127T>C
NM_001127487.1:c.*127T>C (FLNC)	NP_001120959.1:n.*127T>C
NM_001458.4:c.*127T>C , LRG_870t1:c.*127T>C (FLNC)	NP_001449.3:n.*127T>C
NR_149055.1:n.102+3875A>G (FLNC-AS1)
NM_001127487.2:c.*127T>C (FLNC)	NP_001120959.1:n.*127T>C
NM_001458.5:c.*127T>C (FLNC) MANE Select	NP_001449.3:n.*127T>C