Canonical Allele Identifier: CA369208212
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2128938454
MyVariant Identifiers: chr7:g.128491571G>T (hg19) chr7:g.128851517G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851517G>T , CM000669.2:g.128851517G>T GRCh38
NC_000007.13:g.128491571G>T , CM000669.1:g.128491571G>T GRCh37
NC_000007.12:g.128278807G>T NCBI36
NG_011807.1:g.26089G>T , LRG_870:g.26089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5731G>T (FLNC) MANE Select ENSP00000327145.8:p.Asp1911Tyr
ENST00000325888.12:c.5731G>T (FLNC) ENSP00000327145.8:p.Asp1911Tyr
ENST00000346177.6:c.5632G>T (FLNC) ENSP00000344002.6:p.Asp1878Tyr
NM_001127487.1:c.5632G>T (FLNC) NP_001120959.1:p.Asp1878Tyr
NM_001458.4:c.5731G>T , LRG_870t1:c.5731G>T (FLNC) NP_001449.3:p.Asp1911Tyr
NR_149055.1:n.216-17C>A (FLNC-AS1)
NM_001127487.2:c.5632G>T (FLNC) NP_001120959.1:p.Asp1878Tyr
NM_001458.5:c.5731G>T (FLNC) MANE Select NP_001449.3:p.Asp1911Tyr
Search 100 bp 5'
Search 100 bp 3'