Canonical Allele Identifier: CA2695220673
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485465del , CM000677.2:g.48485465del GRCh38
NC_000015.9:g.48777662del , CM000677.1:g.48777662del GRCh37
NC_000015.8:g.46564954del NCBI36
NG_008805.2:g.165325del , LRG_778:g.165325del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3622del ENSP00000453958.2:p.Cys1208ValfsTer22
ENST00000674301.2:c.3622del ENSP00000501333.2:p.Cys1208ValfsTer22
ENST00000684448.1:n.2296del
ENST00000316623.10:c.3622del MANE Select ENSP00000325527.5:p.Cys1208ValfsTer22
ENST00000316623.9:c.3622del ENSP00000325527.5:p.Cys1208ValfsTer22
ENST00000537463.6:c.637-10814del ENSP00000440294.2:n.637-10814del
NM_000138.4:c.3622del , LRG_778t1:c.3622del NP_000129.3:p.Cys1208ValfsTer22
NM_000138.5:c.3622del MANE Select NP_000129.3:p.Cys1208ValfsTer22