Canonical Allele Identifier: CA166196806

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs867483871
• MyVariant Identifiers: chr7:g.128498679G>A (hg19) ; chr7:g.128858625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858625G>A , CM000669.2:g.128858625G>A	GRCh38
NC_000007.13:g.128498679G>A , CM000669.1:g.128498679G>A	GRCh37
NC_000007.12:g.128285915G>A	NCBI36
NG_011807.1:g.33197G>A , LRG_870:g.33197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*102G>A (FLNC) MANE Select	ENSP00000327145.8:n.*102G>A
ENST00000325888.12:c.*102G>A (FLNC)	ENSP00000327145.8:n.*102G>A
ENST00000346177.6:c.*102G>A (FLNC)	ENSP00000344002.6:n.*102G>A
NM_001127487.1:c.*102G>A (FLNC)	NP_001120959.1:n.*102G>A
NM_001458.4:c.*102G>A , LRG_870t1:c.*102G>A (FLNC)	NP_001449.3:n.*102G>A
NR_149055.1:n.102+3900C>T (FLNC-AS1)
NM_001127487.2:c.*102G>A (FLNC)	NP_001120959.1:n.*102G>A
NM_001458.5:c.*102G>A (FLNC) MANE Select	NP_001449.3:n.*102G>A