Canonical Allele Identifier: CA017854
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42448
ClinVar RCV Id: RCV000035294
dbSNP Id: rs397515867

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48526164dup , CM000677.2:g.48526164dup GRCh38
NC_000015.9:g.48818361dup , CM000677.1:g.48818361dup GRCh37
NC_000015.8:g.46605653dup NCBI36
NG_008805.2:g.124629dup , LRG_778:g.124629dup

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.958dup ENSP00000453958.2:p.Tyr320LeufsTer28
ENST00000674301.2:c.958dup ENSP00000501333.2:p.Tyr320LeufsTer28
ENST00000316623.10:c.958dup MANE Select ENSP00000325527.5:p.Tyr320LeufsTer28
ENST00000316623.9:c.958dup ENSP00000325527.5:p.Tyr320LeufsTer28
ENST00000537463.6:c.636+11551dup ENSP00000440294.2:n.636+11551dup
NM_000138.4:c.958dup , LRG_778t1:c.958dup NP_000129.3:p.Tyr320LeufsTer28
NM_000138.5:c.958dup MANE Select NP_000129.3:p.Tyr320LeufsTer28