Canonical Allele Identifier: CA392323398

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415736G>T , CM000677.2:g.48415736G>T	GRCh38
NC_000015.9:g.48707933G>T , CM000677.1:g.48707933G>T	GRCh37
NC_000015.8:g.46495225G>T	NCBI36
NG_008805.2:g.235053C>A , LRG_778:g.235053C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7851C>A MANE Select	NP_000129.3:p.Cys2617Ter
ENST00000316623.10:c.7851C>A MANE Select	ENSP00000325527.5:p.Cys2617Ter
NM_000138.4:c.7851C>A , LRG_778t1:c.7851C>A	NP_000129.3:p.Cys2617Ter
ENST00000316623.9:c.7851C>A	ENSP00000325527.5:p.Cys2617Ter
ENST00000559133.5:c.3220C>A
ENST00000559133.6:c.*659C>A	ENSP00000453958.2:n.*659C>A
ENST00000561429.1:n.106C>A
ENST00000674301.1:c.3017C>A	ENSP00000501333.1:n.3017C>A
ENST00000674301.2:c.*1364C>A	ENSP00000501333.2:n.*1364C>A
ENST00000682158.1:n.1232C>A
ENST00000682170.1:n.2032C>A
ENST00000682767.1:n.1148C>A