Canonical Allele Identifier: CA2695220343
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48510125_48510129del , CM000677.2:g.48510125_48510129del GRCh38
NC_000015.9:g.48802322_48802326del , CM000677.1:g.48802322_48802326del GRCh37
NC_000015.8:g.46589614_46589618del NCBI36
NG_008805.2:g.140660_140664del , LRG_778:g.140660_140664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1629_1633del ENSP00000453958.2:p.Asn543LysfsTer14
ENST00000674301.2:c.1629_1633del ENSP00000501333.2:p.Asn543LysfsTer14
ENST00000684448.1:n.303_307del
ENST00000316623.10:c.1629_1633del MANE Select ENSP00000325527.5:p.Asn543LysfsTer14
ENST00000316623.9:c.1629_1633del ENSP00000325527.5:p.Asn543LysfsTer14
ENST00000537463.6:c.636+27582_636+27586del ENSP00000440294.2:n.636+27582_636+27586del
NM_000138.4:c.1629_1633del , LRG_778t1:c.1629_1633del NP_000129.3:p.Asn543LysfsTer14
NM_000138.5:c.1629_1633del MANE Select NP_000129.3:p.Asn543LysfsTer14