Canonical Allele Identifier: CA2695220535
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48463949del , CM000677.2:g.48463949del GRCh38
NC_000015.9:g.48756146del , CM000677.1:g.48756146del GRCh37
NC_000015.8:g.46543438del NCBI36
NG_008805.2:g.186840del , LRG_778:g.186840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5015del ENSP00000453958.2:p.Cys1672LeufsTer10
ENST00000674301.2:c.5015del ENSP00000501333.2:p.Cys1672LeufsTer10
ENST00000684448.1:n.3689del
ENST00000316623.10:c.5015del MANE Select ENSP00000325527.5:p.Cys1672LeufsTer10
ENST00000674301.1:c.14del ENSP00000501333.1:p.Cys5LeufsTer10
ENST00000316623.9:c.5015del ENSP00000325527.5:p.Cys1672LeufsTer10
ENST00000537463.6:c.*778del ENSP00000440294.2:n.*778del
ENST00000559133.5:c.322del
NM_000138.4:c.5015del , LRG_778t1:c.5015del NP_000129.3:p.Cys1672LeufsTer10
NM_000138.5:c.5015del MANE Select NP_000129.3:p.Cys1672LeufsTer10