Canonical Allele Identifier: CA392319781

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703502A>T (hg19) ; chr15:g.48411305A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411305A>T , CM000677.2:g.48411305A>T	GRCh38
NC_000015.9:g.48703502A>T , CM000677.1:g.48703502A>T	GRCh37
NC_000015.8:g.46490794A>T	NCBI36
NG_008805.2:g.239484T>A , LRG_778:g.239484T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1109T>A	ENSP00000453958.2:n.*1109T>A
ENST00000674301.2:c.*1814T>A	ENSP00000501333.2:n.*1814T>A
ENST00000682158.1:n.1682T>A
ENST00000682170.1:n.2482T>A
ENST00000682767.1:n.1598T>A
ENST00000316623.10:c.8301T>A MANE Select	ENSP00000325527.5:p.Asn2767Lys
ENST00000674301.1:c.3467T>A	ENSP00000501333.1:n.3467T>A
ENST00000316623.9:c.8301T>A	ENSP00000325527.5:p.Asn2767Lys
ENST00000559133.5:c.3670T>A
ENST00000561429.1:n.556T>A
NM_000138.4:c.8301T>A , LRG_778t1:c.8301T>A	NP_000129.3:p.Asn2767Lys
NM_000138.5:c.8301T>A MANE Select	NP_000129.3:p.Asn2767Lys