Canonical Allele Identifier: CA369198283

Gene: FLNC

Linked Data

• MyVariant Identifiers: chr7:g.128486042A>G (hg19) ; chr7:g.128845988A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128845988A>G , CM000669.2:g.128845988A>G	GRCh38
NC_000007.13:g.128486042A>G , CM000669.1:g.128486042A>G	GRCh37
NC_000007.12:g.128273278A>G	NCBI36
NG_011807.1:g.20560A>G , LRG_870:g.20560A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.3791-2A>G MANE Select	ENSP00000327145.8:n.3791-2A>G
ENST00000325888.12:c.3791-2A>G	ENSP00000327145.8:n.3791-2A>G
ENST00000346177.6:c.3791-2A>G	ENSP00000344002.6:n.3791-2A>G
NM_001127487.1:c.3791-2A>G	NP_001120959.1:n.3791-2A>G
NM_001458.4:c.3791-2A>G , LRG_870t1:c.3791-2A>G	NP_001449.3:n.3791-2A>G
NM_001127487.2:c.3791-2A>G	NP_001120959.1:n.3791-2A>G
NM_001458.5:c.3791-2A>G MANE Select	NP_001449.3:n.3791-2A>G