Canonical Allele Identifier: CA1742581354

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843754_128843755delinsCT , CM000669.2:g.128843754_128843755delinsCT	GRCh38
NC_000007.13:g.128483808_128483809delinsCT , CM000669.1:g.128483808_128483809delinsCT	GRCh37
NC_000007.12:g.128271044_128271045delinsCT	NCBI36
NG_011807.1:g.18326_18327delinsCT , LRG_870:g.18326_18327delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2812-42_2812-41delinsCT MANE Select	ENSP00000327145.8:n.2812-42_2812-41delinsCT
ENST00000325888.12:c.2812-42_2812-41delinsCT	ENSP00000327145.8:n.2812-42_2812-41delinsCT
ENST00000346177.6:c.2812-42_2812-41delinsCT	ENSP00000344002.6:n.2812-42_2812-41delinsCT
NM_001127487.1:c.2812-42_2812-41delinsCT	NP_001120959.1:n.2812-42_2812-41delinsCT
NM_001458.4:c.2812-42_2812-41delinsCT , LRG_870t1:c.2812-42_2812-41delinsCT	NP_001449.3:n.2812-42_2812-41delinsCT
NM_001127487.2:c.2812-42_2812-41delinsCT	NP_001120959.1:n.2812-42_2812-41delinsCT
NM_001458.5:c.2812-42_2812-41delinsCT MANE Select	NP_001449.3:n.2812-42_2812-41delinsCT