Canonical Allele Identifier: CA833134445

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1220063228
• gnomAD v3: 7-128856371-G-C
• gnomAD v4: 7-128856371-G-C
• MyVariant Identifiers: chr7:g.128496425G>C (hg19) ; chr7:g.128856371G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128856371G>C , CM000669.2:g.128856371G>C	GRCh38
NC_000007.13:g.128496425G>C , CM000669.1:g.128496425G>C	GRCh37
NC_000007.12:g.128283661G>C	NCBI36
NG_011807.1:g.30943G>C , LRG_870:g.30943G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7252-147G>C (FLNC) MANE Select	ENSP00000327145.8:n.7252-147G>C
ENST00000325888.12:c.7252-147G>C (FLNC)	ENSP00000327145.8:n.7252-147G>C
ENST00000346177.6:c.7153-147G>C (FLNC)	ENSP00000344002.6:n.7153-147G>C
NM_001127487.1:c.7153-147G>C (FLNC)	NP_001120959.1:n.7153-147G>C
NM_001458.4:c.7252-147G>C , LRG_870t1:c.7252-147G>C (FLNC)	NP_001449.3:n.7252-147G>C
NR_149055.1:n.103-2974C>G (FLNC-AS1)
NM_001127487.2:c.7153-147G>C (FLNC)	NP_001120959.1:n.7153-147G>C
NM_001458.5:c.7252-147G>C (FLNC) MANE Select	NP_001449.3:n.7252-147G>C