Canonical Allele Identifier: CA369221235
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128498426A>C (hg19) chr7:g.128858372A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858372A>C , CM000669.2:g.128858372A>C GRCh38
NC_000007.13:g.128498426A>C , CM000669.1:g.128498426A>C GRCh37
NC_000007.12:g.128285662A>C NCBI36
NG_011807.1:g.32944A>C , LRG_870:g.32944A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8027A>C (FLNC) MANE Select ENSP00000327145.8:p.Lys2676Thr
ENST00000325888.12:c.8027A>C (FLNC) ENSP00000327145.8:p.Lys2676Thr
ENST00000346177.6:c.7928A>C (FLNC) ENSP00000344002.6:p.Lys2643Thr
NM_001127487.1:c.7928A>C (FLNC) NP_001120959.1:p.Lys2643Thr
NM_001458.4:c.8027A>C , LRG_870t1:c.8027A>C (FLNC) NP_001449.3:p.Lys2676Thr
NR_149055.1:n.102+4153T>G (FLNC-AS1)
NM_001127487.2:c.7928A>C (FLNC) NP_001120959.1:p.Lys2643Thr
NM_001458.5:c.8027A>C (FLNC) MANE Select NP_001449.3:p.Lys2676Thr
Search 100 bp 5'
Search 100 bp 3'