Canonical Allele Identifier: CA713379587
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1231510349

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411493del , CM000677.2:g.48411493del GRCh38
NC_000015.9:g.48703690del , CM000677.1:g.48703690del GRCh37
NC_000015.8:g.46490982del NCBI36
NG_008805.2:g.239296del , LRG_778:g.239296del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-114del ENSP00000453958.2:n.*1035-114del
ENST00000674301.2:c.*1740-114del ENSP00000501333.2:n.*1740-114del
ENST00000682158.1:n.1608-114del
ENST00000682170.1:n.2408-114del
ENST00000682767.1:n.1524-114del
ENST00000316623.10:c.8227-114del MANE Select ENSP00000325527.5:n.8227-114del
ENST00000674301.1:c.3393-114del ENSP00000501333.1:n.3393-114del
ENST00000316623.9:c.8227-114del ENSP00000325527.5:n.8227-114del
ENST00000559133.5:c.3596-114del
ENST00000561429.1:n.482-114del
NM_000138.4:c.8227-114del , LRG_778t1:c.8227-114del NP_000129.3:n.8227-114del
NM_000138.5:c.8227-114del MANE Select NP_000129.3:n.8227-114del