Canonical Allele Identifier: CA2175489362
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2042896694

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415599dup , CM000677.2:g.48415599dup GRCh38
NC_000015.9:g.48707796dup , CM000677.1:g.48707796dup GRCh37
NC_000015.8:g.46495088dup NCBI36
NG_008805.2:g.235190dup , LRG_778:g.235190dup

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*796dup ENSP00000453958.2:n.*796dup
ENST00000674301.2:c.*1501dup ENSP00000501333.2:n.*1501dup
ENST00000682158.1:n.1369dup
ENST00000682170.1:n.2169dup
ENST00000682767.1:n.1285dup
ENST00000316623.10:c.7988dup MANE Select ENSP00000325527.5:p.Cys2663TrpfsTer?
ENST00000674301.1:c.3154dup ENSP00000501333.1:n.3154dup
ENST00000316623.9:c.7988dup ENSP00000325527.5:p.Cys2663TrpfsTer?
ENST00000559133.5:c.3357dup
ENST00000561429.1:n.243dup
NM_000138.4:c.7988dup , LRG_778t1:c.7988dup NP_000129.3:p.Cys2663TrpfsTer?
NM_000138.5:c.7988dup MANE Select NP_000129.3:p.Cys2663TrpfsTer?