Canonical Allele Identifier: CA017730
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 36131
ClinVar RCV Id: RCV000029794
dbSNP Id: rs193922246

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411190_48411195del , CM000677.2:g.48411190_48411195del GRCh38
NC_000015.9:g.48703387_48703392del , CM000677.1:g.48703387_48703392del GRCh37
NC_000015.8:g.46490679_46490684del NCBI36
NG_008805.2:g.239595_239600del , LRG_778:g.239595_239600del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1220_*1225del ENSP00000453958.2:n.*1220_*1225del
ENST00000674301.2:c.*1925_*1930del ENSP00000501333.2:n.*1925_*1930del
ENST00000682158.1:n.1793_1798del
ENST00000682170.1:n.2593_2598del
ENST00000682767.1:n.1709_1714del
ENST00000316623.10:c.8412_8417del MANE Select ENSP00000325527.5:p.Lys2805_Ile2806del
ENST00000674301.1:c.3578_3583del ENSP00000501333.1:n.3578_3583del
ENST00000316623.9:c.8412_8417del ENSP00000325527.5:p.Lys2805_Ile2806del
ENST00000559133.5:c.3781_3786del
NM_000138.4:c.8412_8417del , LRG_778t1:c.8412_8417del NP_000129.3:p.Lys2805_Ile2806del
NM_000138.5:c.8412_8417del MANE Select NP_000129.3:p.Lys2805_Ile2806del