Canonical Allele Identifier: CA1742544685

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837497_128837499delinsCCT , CM000669.2:g.128837497_128837499delinsCCT	GRCh38
NC_000007.13:g.128477551_128477553delinsCCT , CM000669.1:g.128477551_128477553delinsCCT	GRCh37
NC_000007.12:g.128264787_128264789delinsCCT	NCBI36
NG_011807.1:g.12069_12071delinsCCT , LRG_870:g.12069_12071delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.799_801delinsCCT MANE Select	ENSP00000327145.8:p.Pro267=
ENST00000325888.12:c.799_801delinsCCT	ENSP00000327145.8:p.Pro267=
ENST00000346177.6:c.799_801delinsCCT	ENSP00000344002.6:p.Pro267=
NM_001127487.1:c.799_801delinsCCT	NP_001120959.1:p.Pro267=
NM_001458.4:c.799_801delinsCCT , LRG_870t1:c.799_801delinsCCT	NP_001449.3:p.Pro267=
NM_001127487.2:c.799_801delinsCCT	NP_001120959.1:p.Pro267=
NM_001458.5:c.799_801delinsCCT MANE Select	NP_001449.3:p.Pro267=