Canonical Allele Identifier: CA369220269
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs775543867
MyVariant Identifiers: chr7:g.128498155A>G (hg19) chr7:g.128858101A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858101A>G , CM000669.2:g.128858101A>G GRCh38
NC_000007.13:g.128498155A>G , CM000669.1:g.128498155A>G GRCh37
NC_000007.12:g.128285391A>G NCBI36
NG_011807.1:g.32673A>G , LRG_870:g.32673A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7874A>G (FLNC) MANE Select ENSP00000327145.8:p.Tyr2625Cys
ENST00000325888.12:c.7874A>G (FLNC) ENSP00000327145.8:p.Tyr2625Cys
ENST00000346177.6:c.7775A>G (FLNC) ENSP00000344002.6:p.Tyr2592Cys
NM_001127487.1:c.7775A>G (FLNC) NP_001120959.1:p.Tyr2592Cys
NM_001458.4:c.7874A>G , LRG_870t1:c.7874A>G (FLNC) NP_001449.3:p.Tyr2625Cys
NR_149055.1:n.102+4424T>C (FLNC-AS1)
NM_001127487.2:c.7775A>G (FLNC) NP_001120959.1:p.Tyr2592Cys
NM_001458.5:c.7874A>G (FLNC) MANE Select NP_001449.3:p.Tyr2625Cys
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Search 100 bp 3'