Canonical Allele Identifier: CA4475362
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2146708
ClinVar RCV Id: RCV003076812
dbSNP Id: rs748829335
ExAC: 7:128488047 C / T
gnomAD v2: 7-128488047-C-T
gnomAD v3: 7-128847993-C-T
gnomAD v4: 7-128847993-C-T
MyVariant Identifiers: chr7:g.128488047C>T (hg19) chr7:g.128847993C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847993C>T , CM000669.2:g.128847993C>T GRCh38
NC_000007.13:g.128488047C>T , CM000669.1:g.128488047C>T GRCh37
NC_000007.12:g.128275283C>T NCBI36
NG_011807.1:g.22565C>T , LRG_870:g.22565C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4505C>T MANE Select ENSP00000327145.8:p.Thr1502Ile
ENST00000325888.12:c.4505C>T ENSP00000327145.8:p.Thr1502Ile
ENST00000346177.6:c.4505C>T ENSP00000344002.6:p.Thr1502Ile
NM_001127487.1:c.4505C>T NP_001120959.1:p.Thr1502Ile
NM_001458.4:c.4505C>T , LRG_870t1:c.4505C>T NP_001449.3:p.Thr1502Ile
NM_001127487.2:c.4505C>T NP_001120959.1:p.Thr1502Ile
NM_001458.5:c.4505C>T MANE Select NP_001449.3:p.Thr1502Ile
Search 100 bp 5'
Search 100 bp 3'