Canonical Allele Identifier: CA490119025

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703529A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411332A>T , CM000677.2:g.48411332A>T	GRCh38
NC_000015.9:g.48703529A>T , CM000677.1:g.48703529A>T	GRCh37
NC_000015.8:g.46490821A>T	NCBI36
NG_008805.2:g.239457T>A , LRG_778:g.239457T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1082T>A	ENSP00000453958.2:n.*1082T>A
ENST00000674301.2:c.*1787T>A	ENSP00000501333.2:n.*1787T>A
ENST00000682158.1:n.1655T>A
ENST00000682170.1:n.2455T>A
ENST00000682767.1:n.1571T>A
ENST00000316623.10:c.8274T>A MANE Select	ENSP00000325527.5:p.Val2758=
ENST00000674301.1:c.3440T>A	ENSP00000501333.1:n.3440T>A
ENST00000316623.9:c.8274T>A	ENSP00000325527.5:p.Val2758=
ENST00000559133.5:c.3643T>A
ENST00000561429.1:n.529T>A
NM_000138.4:c.8274T>A , LRG_778t1:c.8274T>A	NP_000129.3:p.Val2758=
NM_000138.5:c.8274T>A MANE Select	NP_000129.3:p.Val2758=