Canonical Allele Identifier: CA2580089535
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748892
ClinVar RCV Id: RCV002345221

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448774_48448782delinsGC , CM000677.2:g.48448774_48448782delinsGC GRCh38
NC_000015.9:g.48740971_48740979delinsGC , CM000677.1:g.48740971_48740979delinsGC GRCh37
NC_000015.8:g.46528263_46528271delinsGC NCBI36
NG_008805.2:g.202007_202015delinsGC , LRG_778:g.202007_202015delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.5657_5665delinsGC ENSP00000453958.2:p.Gln1886ArgfsTer5
ENST00000674301.2:c.5657_5665delinsGC ENSP00000501333.2:p.Gln1886ArgfsTer5
ENST00000684448.1:n.4331_4339delinsGC
ENST00000316623.10:c.5657_5665delinsGC MANE Select ENSP00000325527.5:p.Gln1886ArgfsTer5
ENST00000674301.1:c.656_664delinsGC ENSP00000501333.1:p.Gln219ArgfsTer5
ENST00000316623.9:c.5657_5665delinsGC ENSP00000325527.5:p.Gln1886ArgfsTer5
ENST00000537463.6:c.*1420_*1428delinsGC ENSP00000440294.2:n.*1420_*1428delinsGC
ENST00000559133.5:c.964_972delinsGC
NM_000138.4:c.5657_5665delinsGC , LRG_778t1:c.5657_5665delinsGC NP_000129.3:p.Gln1886ArgfsTer5
NM_000138.5:c.5657_5665delinsGC MANE Select NP_000129.3:p.Gln1886ArgfsTer5