Canonical Allele Identifier: CA369197259

Gene: FLNC

Linked Data

• dbSNP Id: rs1475328592
• gnomAD v2: 7-128485088-T-C
• gnomAD v4: 7-128845034-T-C
• MyVariant Identifiers: chr7:g.128485088T>C (hg19) ; chr7:g.128845034T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128845034T>C , CM000669.2:g.128845034T>C	GRCh38
NC_000007.13:g.128485088T>C , CM000669.1:g.128485088T>C	GRCh37
NC_000007.12:g.128272324T>C	NCBI36
NG_011807.1:g.19606T>C , LRG_870:g.19606T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.3569T>C MANE Select	ENSP00000327145.8:p.Ile1190Thr
ENST00000325888.12:c.3569T>C	ENSP00000327145.8:p.Ile1190Thr
ENST00000346177.6:c.3569T>C	ENSP00000344002.6:p.Ile1190Thr
NM_001127487.1:c.3569T>C	NP_001120959.1:p.Ile1190Thr
NM_001458.4:c.3569T>C , LRG_870t1:c.3569T>C	NP_001449.3:p.Ile1190Thr
NM_001127487.2:c.3569T>C	NP_001120959.1:p.Ile1190Thr
NM_001458.5:c.3569T>C MANE Select	NP_001449.3:p.Ile1190Thr