Canonical Allele Identifier: CA2777853550

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853839_128853840insGGTTCC , CM000669.2:g.128853839_128853840insGGTTCC	GRCh38
NC_000007.13:g.128493893_128493894insGGTTCC , CM000669.1:g.128493893_128493894insGGTTCC	GRCh37
NC_000007.12:g.128281129_128281130insGGTTCC	NCBI36
NG_011807.1:g.28411_28412insGGTTCC , LRG_870:g.28411_28412insGGTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6484+2_6484+3insGGTTCC (FLNC) MANE Select	ENSP00000327145.8:n.6484+2_6484+3insGGTTCC
ENST00000325888.12:c.6484+2_6484+3insGGTTCC (FLNC)	ENSP00000327145.8:n.6484+2_6484+3insGGTTCC
ENST00000346177.6:c.6385+2_6385+3insGGTTCC (FLNC)	ENSP00000344002.6:n.6385+2_6385+3insGGTTCC
NM_001127487.1:c.6385+2_6385+3insGGTTCC (FLNC)	NP_001120959.1:n.6385+2_6385+3insGGTTCC
NM_001458.4:c.6484+2_6484+3insGGTTCC , LRG_870t1:c.6484+2_6484+3insGGTTCC (FLNC)	NP_001449.3:n.6484+2_6484+3insGGTTCC
NR_149055.1:n.103-443_103-442insGGAACC (FLNC-AS1)
NM_001127487.2:c.6385+2_6385+3insGGTTCC (FLNC)	NP_001120959.1:n.6385+2_6385+3insGGTTCC
NM_001458.5:c.6484+2_6484+3insGGTTCC (FLNC) MANE Select	NP_001449.3:n.6484+2_6484+3insGGTTCC