Canonical Allele Identifier: CA713383749
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1439210093

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485259dup , CM000677.2:g.48485259dup GRCh38
NC_000015.9:g.48777456dup , CM000677.1:g.48777456dup GRCh37
NC_000015.8:g.46564748dup NCBI36
NG_008805.2:g.165533dup , LRG_778:g.165533dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3712+118dup ENSP00000453958.2:n.3712+118dup
ENST00000674301.2:c.3712+118dup ENSP00000501333.2:n.3712+118dup
ENST00000684448.1:n.2386+118dup
ENST00000316623.10:c.3712+118dup MANE Select ENSP00000325527.5:n.3712+118dup
ENST00000316623.9:c.3712+118dup ENSP00000325527.5:n.3712+118dup
ENST00000537463.6:c.637-10606dup ENSP00000440294.2:n.637-10606dup
NM_000138.4:c.3712+118dup , LRG_778t1:c.3712+118dup NP_000129.3:n.3712+118dup
NM_000138.5:c.3712+118dup MANE Select NP_000129.3:n.3712+118dup