Canonical Allele Identifier: CA369216553

Gene: FLNC FLNC-AS1

Linked Data

• MyVariant Identifiers: chr7:g.128496605T>C (hg19) ; chr7:g.128856551T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128856551T>C , CM000669.2:g.128856551T>C	GRCh38
NC_000007.13:g.128496605T>C , CM000669.1:g.128496605T>C	GRCh37
NC_000007.12:g.128283841T>C	NCBI36
NG_011807.1:g.31123T>C , LRG_870:g.31123T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.7285T>C (FLNC) MANE Select	ENSP00000327145.8:p.Phe2429Leu
ENST00000325888.12:c.7285T>C (FLNC)	ENSP00000327145.8:p.Phe2429Leu
ENST00000346177.6:c.7186T>C (FLNC)	ENSP00000344002.6:p.Phe2396Leu
NM_001127487.1:c.7186T>C (FLNC)	NP_001120959.1:p.Phe2396Leu
NM_001458.4:c.7285T>C , LRG_870t1:c.7285T>C (FLNC)	NP_001449.3:p.Phe2429Leu
NR_149055.1:n.103-3154A>G (FLNC-AS1)
NM_001127487.2:c.7186T>C (FLNC)	NP_001120959.1:p.Phe2396Leu
NM_001458.5:c.7285T>C (FLNC) MANE Select	NP_001449.3:p.Phe2429Leu