Canonical Allele Identifier: CA2175486945
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411484C= , CM000677.2:g.48411484C= GRCh38
NC_000015.9:g.48703681C= , CM000677.1:g.48703681C= GRCh37
NC_000015.8:g.46490973C= NCBI36
NG_008805.2:g.239305G= , LRG_778:g.239305G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-105G= ENSP00000453958.2:n.*1035-105G=
ENST00000674301.2:c.*1740-105G= ENSP00000501333.2:n.*1740-105G=
ENST00000682158.1:n.1608-105G=
ENST00000682170.1:n.2408-105G=
ENST00000682767.1:n.1524-105G=
ENST00000316623.10:c.8227-105G= MANE Select ENSP00000325527.5:n.8227-105G=
ENST00000674301.1:c.3393-105G= ENSP00000501333.1:n.3393-105G=
ENST00000316623.9:c.8227-105G= ENSP00000325527.5:n.8227-105G=
ENST00000559133.5:c.3596-105G=
ENST00000561429.1:n.482-105G=
NM_000138.4:c.8227-105G= , LRG_778t1:c.8227-105G= NP_000129.3:n.8227-105G=
NM_000138.5:c.8227-105G= MANE Select NP_000129.3:n.8227-105G=