Canonical Allele Identifier: CA2628331595
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428293G>A , CM000677.2:g.48428293G>A GRCh38
NC_000015.9:g.48720490G>A , CM000677.1:g.48720490G>A GRCh37
NC_000015.8:g.46507782G>A NCBI36
NG_008805.2:g.222496C>T , LRG_778:g.222496C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6997+53C>T ENSP00000453958.2:n.6997+53C>T
ENST00000674301.2:c.*448+53C>T ENSP00000501333.2:n.*448+53C>T
ENST00000682170.1:n.659C>T
ENST00000682767.1:n.232+53C>T
ENST00000316623.10:c.6997+53C>T MANE Select ENSP00000325527.5:n.6997+53C>T
ENST00000674301.1:c.2101+53C>T ENSP00000501333.1:n.2101+53C>T
ENST00000316623.9:c.6997+53C>T ENSP00000325527.5:n.6997+53C>T
ENST00000559133.5:c.2304+53C>T
ENST00000560720.1:n.337C>T
NM_000138.4:c.6997+53C>T , LRG_778t1:c.6997+53C>T NP_000129.3:n.6997+53C>T
NM_000138.5:c.6997+53C>T MANE Select NP_000129.3:n.6997+53C>T