Canonical Allele Identifier: CA2846047227

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843396_128843397insCC , CM000669.2:g.128843396_128843397insCC	GRCh38
NC_000007.13:g.128483450_128483451insCC , CM000669.1:g.128483450_128483451insCC	GRCh37
NC_000007.12:g.128270686_128270687insCC	NCBI36
NG_011807.1:g.17968_17969insCC , LRG_870:g.17968_17969insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2642-12_2642-11insCC MANE Select	ENSP00000327145.8:n.2642-12_2642-11insCC
ENST00000325888.12:c.2642-12_2642-11insCC	ENSP00000327145.8:n.2642-12_2642-11insCC
ENST00000346177.6:c.2642-12_2642-11insCC	ENSP00000344002.6:n.2642-12_2642-11insCC
NM_001127487.1:c.2642-12_2642-11insCC	NP_001120959.1:n.2642-12_2642-11insCC
NM_001458.4:c.2642-12_2642-11insCC , LRG_870t1:c.2642-12_2642-11insCC	NP_001449.3:n.2642-12_2642-11insCC
NM_001127487.2:c.2642-12_2642-11insCC	NP_001120959.1:n.2642-12_2642-11insCC
NM_001458.5:c.2642-12_2642-11insCC MANE Select	NP_001449.3:n.2642-12_2642-11insCC