Canonical Allele Identifier: CA457848547

Gene: FLNC

Linked Data

• dbSNP Id: rs1005510680
• gnomAD v2: 7-128487842-G-C
• gnomAD v4: 7-128847788-G-C
• MyVariant Identifiers: chr7:g.128487842G>C (hg19) ; chr7:g.128847788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128847788G>C , CM000669.2:g.128847788G>C	GRCh38
NC_000007.13:g.128487842G>C , CM000669.1:g.128487842G>C	GRCh37
NC_000007.12:g.128275078G>C	NCBI36
NG_011807.1:g.22360G>C , LRG_870:g.22360G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4380G>C MANE Select	ENSP00000327145.8:p.Arg1460=
ENST00000325888.12:c.4380G>C	ENSP00000327145.8:p.Arg1460=
ENST00000346177.6:c.4380G>C	ENSP00000344002.6:p.Arg1460=
NM_001127487.1:c.4380G>C	NP_001120959.1:p.Arg1460=
NM_001458.4:c.4380G>C , LRG_870t1:c.4380G>C	NP_001449.3:p.Arg1460=
NM_001127487.2:c.4380G>C	NP_001120959.1:p.Arg1460=
NM_001458.5:c.4380G>C MANE Select	NP_001449.3:p.Arg1460=