Canonical Allele Identifier: CA1742589284

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128847745_128847748delinsTGAA , CM000669.2:g.128847745_128847748delinsTGAA	GRCh38
NC_000007.13:g.128487799_128487802delinsTGAA , CM000669.1:g.128487799_128487802delinsTGAA	GRCh37
NC_000007.12:g.128275035_128275038delinsTGAA	NCBI36
NG_011807.1:g.22317_22320delinsTGAA , LRG_870:g.22317_22320delinsTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4337_4340delinsTGAA MANE Select	ENSP00000327145.8:p.Val1446=
ENST00000325888.12:c.4337_4340delinsTGAA	ENSP00000327145.8:p.Val1446=
ENST00000346177.6:c.4337_4340delinsTGAA	ENSP00000344002.6:p.Val1446=
NM_001127487.1:c.4337_4340delinsTGAA	NP_001120959.1:p.Val1446=
NM_001458.4:c.4337_4340delinsTGAA , LRG_870t1:c.4337_4340delinsTGAA	NP_001449.3:p.Val1446=
NM_001127487.2:c.4337_4340delinsTGAA	NP_001120959.1:p.Val1446=
NM_001458.5:c.4337_4340delinsTGAA MANE Select	NP_001449.3:p.Val1446=