Canonical Allele Identifier: CA392319875

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703513A>T (hg19) ; chr15:g.48411316A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411316A>T , CM000677.2:g.48411316A>T	GRCh38
NC_000015.9:g.48703513A>T , CM000677.1:g.48703513A>T	GRCh37
NC_000015.8:g.46490805A>T	NCBI36
NG_008805.2:g.239473T>A , LRG_778:g.239473T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1098T>A	ENSP00000453958.2:n.*1098T>A
ENST00000674301.2:c.*1803T>A	ENSP00000501333.2:n.*1803T>A
ENST00000682158.1:n.1671T>A
ENST00000682170.1:n.2471T>A
ENST00000682767.1:n.1587T>A
ENST00000316623.10:c.8290T>A MANE Select	ENSP00000325527.5:p.Phe2764Ile
ENST00000674301.1:c.3456T>A	ENSP00000501333.1:n.3456T>A
ENST00000316623.9:c.8290T>A	ENSP00000325527.5:p.Phe2764Ile
ENST00000559133.5:c.3659T>A
ENST00000561429.1:n.545T>A
NM_000138.4:c.8290T>A , LRG_778t1:c.8290T>A	NP_000129.3:p.Phe2764Ile
NM_000138.5:c.8290T>A MANE Select	NP_000129.3:p.Phe2764Ile