Canonical Allele Identifier: CA353659
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222619
ClinVar RCV Id: RCV000208330
dbSNP Id: rs869025420

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48508676_48508677del , CM000677.2:g.48508676_48508677del GRCh38
NC_000015.9:g.48800873_48800874del , CM000677.1:g.48800873_48800874del GRCh37
NC_000015.8:g.46588165_46588166del NCBI36
NG_008805.2:g.142114_142115del , LRG_778:g.142114_142115del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.1744_1745del ENSP00000453958.2:p.Cys582ProfsTer2
ENST00000674301.2:c.1744_1745del ENSP00000501333.2:p.Cys582ProfsTer2
ENST00000684448.1:n.418_419del
ENST00000316623.10:c.1744_1745del MANE Select ENSP00000325527.5:p.Cys582ProfsTer2
ENST00000316623.9:c.1744_1745del ENSP00000325527.5:p.Cys582ProfsTer2
ENST00000537463.6:c.636+29036_636+29037del ENSP00000440294.2:n.636+29036_636+29037de...
NM_000138.4:c.1744_1745del , LRG_778t1:c.1744_1745del NP_000129.3:p.Cys582ProfsTer2
NM_000138.5:c.1744_1745del MANE Select NP_000129.3:p.Cys582ProfsTer2