Canonical Allele Identifier: CA369219642
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128497288G>T (hg19) chr7:g.128857234G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857234G>T , CM000669.2:g.128857234G>T GRCh38
NC_000007.13:g.128497288G>T , CM000669.1:g.128497288G>T GRCh37
NC_000007.12:g.128284524G>T NCBI36
NG_011807.1:g.31806G>T , LRG_870:g.31806G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7678G>T (FLNC) MANE Select ENSP00000327145.8:p.Val2560Leu
ENST00000325888.12:c.7678G>T (FLNC) ENSP00000327145.8:p.Val2560Leu
ENST00000346177.6:c.7579G>T (FLNC) ENSP00000344002.6:p.Val2527Leu
NM_001127487.1:c.7579G>T (FLNC) NP_001120959.1:p.Val2527Leu
NM_001458.4:c.7678G>T , LRG_870t1:c.7678G>T (FLNC) NP_001449.3:p.Val2560Leu
NR_149055.1:n.103-3837C>A (FLNC-AS1)
NM_001127487.2:c.7579G>T (FLNC) NP_001120959.1:p.Val2527Leu
NM_001458.5:c.7678G>T (FLNC) MANE Select NP_001449.3:p.Val2560Leu
Search 100 bp 5'
Search 100 bp 3'