Canonical Allele Identifier: CA341843
Gene: FLNB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58136020_58136022del , CM000665.2:g.58136020_58136022del GRCh38
NC_000003.11:g.58121747_58121749del , CM000665.1:g.58121747_58121749del GRCh37
NC_000003.10:g.58096787_58096789del NCBI36
NG_012801.1:g.132621_132623del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682297.1:n.137_139del
ENST00000682868.1:n.6755_6757del
ENST00000682871.1:c.4806_4808del ENSP00000507805.1:p.Asn1602del
ENST00000684506.1:c.*3338_*3340del ENSP00000507728.1:n.*3338_*3340del
ENST00000684607.1:c.4806_4808del ENSP00000508224.1:p.Asn1602del
ENST00000295956.9:c.4713_4715del MANE Select ENSP00000295956.5:p.Asn1571del
ENST00000295956.8:c.4713_4715del ENSP00000295956.4:p.Asn1571del
ENST00000358537.7:c.4713_4715del ENSP00000351339.3:p.Asn1571del
ENST00000429972.6:c.4713_4715del ENSP00000415599.2:p.Asn1571del
ENST00000481470.5:n.1053_1055del
ENST00000490882.5:c.4806_4808del ENSP00000420213.1:p.Asn1602del
ENST00000493452.5:c.4206_4208del ENSP00000418510.1:p.Asn1402del
NM_001164317.1:c.4806_4808del NP_001157789.1:p.Asn1602del
NM_001164318.1:c.4713_4715del NP_001157790.1:p.Asn1571del
NM_001164319.1:c.4713_4715del NP_001157791.1:p.Asn1571del
NM_001457.3:c.4713_4715del NP_001448.2:p.Asn1571del
XM_005264977.1:c.4806_4808del XP_005265034.1:p.Asn1602del
XM_005264978.1:c.4806_4808del XP_005265035.1:p.Asn1602del
XM_005264981.1:c.4806_4808del XP_005265038.1:p.Asn1602del
XR_940396.1:n.4951_4953del
XM_005264978.2:c.4806_4808del XP_005265035.1:p.Asn1602del
XR_001740065.1:n.4951_4953del
XR_940396.2:n.4951_4953del
NM_001164317.2:c.4806_4808del NP_001157789.1:p.Asn1602del
NM_001164318.2:c.4713_4715del NP_001157790.1:p.Asn1571del
NM_001164319.2:c.4713_4715del NP_001157791.1:p.Asn1571del
NM_001457.4:c.4713_4715del MANE Select NP_001448.2:p.Asn1571del
Search 100 bp 5'
Search 100 bp 3'