Canonical Allele Identifier: CA578150606

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1212015007
• gnomAD v2: 7-128491452-C-T
• gnomAD v4: 7-128851398-C-T
• MyVariant Identifiers: chr7:g.128491452C>T (hg19) ; chr7:g.128851398C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851398C>T , CM000669.2:g.128851398C>T	GRCh38
NC_000007.13:g.128491452C>T , CM000669.1:g.128491452C>T	GRCh37
NC_000007.12:g.128278688C>T	NCBI36
NG_011807.1:g.25970C>T , LRG_870:g.25970C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.5668+38C>T (FLNC) MANE Select	ENSP00000327145.8:n.5668+38C>T
ENST00000325888.12:c.5668+38C>T (FLNC)	ENSP00000327145.8:n.5668+38C>T
ENST00000346177.6:c.5569+38C>T (FLNC)	ENSP00000344002.6:n.5569+38C>T
NM_001127487.1:c.5569+38C>T (FLNC)	NP_001120959.1:n.5569+38C>T
NM_001458.4:c.5668+38C>T , LRG_870t1:c.5668+38C>T (FLNC)	NP_001449.3:n.5668+38C>T
NR_149055.1:n.315+3G>A (FLNC-AS1)
NM_001127487.2:c.5569+38C>T (FLNC)	NP_001120959.1:n.5569+38C>T
NM_001458.5:c.5668+38C>T (FLNC) MANE Select	NP_001449.3:n.5668+38C>T