Canonical Allele Identifier: CA4474025
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1640859
ClinVar RCV Id: RCV002139979
dbSNP Id: rs758484139
ExAC: 7:128475376 G / T
gnomAD v2: 7-128475376-G-T
gnomAD v4: 7-128835322-G-T
MyVariant Identifiers: chr7:g.128475376G>T (hg19) chr7:g.128835322G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835322G>T , CM000669.2:g.128835322G>T GRCh38
NC_000007.13:g.128475376G>T , CM000669.1:g.128475376G>T GRCh37
NC_000007.12:g.128262612G>T NCBI36
NG_011807.1:g.9894G>T , LRG_870:g.9894G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-4G>T MANE Select ENSP00000327145.8:n.353-4G>T
ENST00000325888.12:c.353-4G>T ENSP00000327145.8:n.353-4G>T
ENST00000346177.6:c.353-4G>T ENSP00000344002.6:n.353-4G>T
NM_001127487.1:c.353-4G>T NP_001120959.1:n.353-4G>T
NM_001458.4:c.353-4G>T , LRG_870t1:c.353-4G>T NP_001449.3:n.353-4G>T
NM_001127487.2:c.353-4G>T NP_001120959.1:n.353-4G>T
NM_001458.5:c.353-4G>T MANE Select NP_001449.3:n.353-4G>T
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