Canonical Allele Identifier: CA392319851

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703511A>T (hg19) ; chr15:g.48411314A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411314A>T , CM000677.2:g.48411314A>T	GRCh38
NC_000015.9:g.48703511A>T , CM000677.1:g.48703511A>T	GRCh37
NC_000015.8:g.46490803A>T	NCBI36
NG_008805.2:g.239475T>A , LRG_778:g.239475T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1100T>A	ENSP00000453958.2:n.*1100T>A
ENST00000674301.2:c.*1805T>A	ENSP00000501333.2:n.*1805T>A
ENST00000682158.1:n.1673T>A
ENST00000682170.1:n.2473T>A
ENST00000682767.1:n.1589T>A
ENST00000316623.10:c.8292T>A MANE Select	ENSP00000325527.5:p.Phe2764Leu
ENST00000674301.1:c.3458T>A	ENSP00000501333.1:n.3458T>A
ENST00000316623.9:c.8292T>A	ENSP00000325527.5:p.Phe2764Leu
ENST00000559133.5:c.3661T>A
ENST00000561429.1:n.547T>A
NM_000138.4:c.8292T>A , LRG_778t1:c.8292T>A	NP_000129.3:p.Phe2764Leu
NM_000138.5:c.8292T>A MANE Select	NP_000129.3:p.Phe2764Leu