Canonical Allele Identifier: CA2695220731
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48496133del , CM000677.2:g.48496133del GRCh38
NC_000015.9:g.48788330del , CM000677.1:g.48788330del GRCh37
NC_000015.8:g.46575622del NCBI36
NG_008805.2:g.154658del , LRG_778:g.154658del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2388del ENSP00000453958.2:p.Phe796LeufsTer7
ENST00000674301.2:c.2388del ENSP00000501333.2:p.Phe796LeufsTer7
ENST00000684448.1:n.1062del
ENST00000316623.10:c.2388del MANE Select ENSP00000325527.5:p.Phe796LeufsTer7
ENST00000316623.9:c.2388del ENSP00000325527.5:p.Phe796LeufsTer7
ENST00000537463.6:c.637-21481del ENSP00000440294.2:n.637-21481del
NM_000138.4:c.2388del , LRG_778t1:c.2388del NP_000129.3:p.Phe796LeufsTer7
NM_000138.5:c.2388del MANE Select NP_000129.3:p.Phe796LeufsTer7