Canonical Allele Identifier: CA457577525

Gene: FLNC

Linked Data

• dbSNP Id: rs1391785800
• gnomAD v2: 7-128483372-A-C
• gnomAD v4: 7-128843318-A-C
• MyVariant Identifiers: chr7:g.128483372A>C (hg19) ; chr7:g.128843318A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843318A>C , CM000669.2:g.128843318A>C	GRCh38
NC_000007.13:g.128483372A>C , CM000669.1:g.128483372A>C	GRCh37
NC_000007.12:g.128270608A>C	NCBI36
NG_011807.1:g.17890A>C , LRG_870:g.17890A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.2640A>C MANE Select	ENSP00000327145.8:p.Thr880=
ENST00000325888.12:c.2640A>C	ENSP00000327145.8:p.Thr880=
ENST00000346177.6:c.2640A>C	ENSP00000344002.6:p.Thr880=
NM_001127487.1:c.2640A>C	NP_001120959.1:p.Thr880=
NM_001458.4:c.2640A>C , LRG_870t1:c.2640A>C	NP_001449.3:p.Thr880=
NM_001127487.2:c.2640A>C	NP_001120959.1:p.Thr880=
NM_001458.5:c.2640A>C MANE Select	NP_001449.3:p.Thr880=