Canonical Allele Identifier: CA392322761

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707794A>T (hg19) ; chr15:g.48415597A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415597A>T , CM000677.2:g.48415597A>T	GRCh38
NC_000015.9:g.48707794A>T , CM000677.1:g.48707794A>T	GRCh37
NC_000015.8:g.46495086A>T	NCBI36
NG_008805.2:g.235192T>A , LRG_778:g.235192T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*798T>A	ENSP00000453958.2:n.*798T>A
ENST00000674301.2:c.*1503T>A	ENSP00000501333.2:n.*1503T>A
ENST00000682158.1:n.1371T>A
ENST00000682170.1:n.2171T>A
ENST00000682767.1:n.1287T>A
ENST00000316623.10:c.7990T>A MANE Select	ENSP00000325527.5:p.Ser2664Thr
ENST00000674301.1:c.3156T>A	ENSP00000501333.1:n.3156T>A
ENST00000316623.9:c.7990T>A	ENSP00000325527.5:p.Ser2664Thr
ENST00000559133.5:c.3359T>A
ENST00000561429.1:n.245T>A
NM_000138.4:c.7990T>A , LRG_778t1:c.7990T>A	NP_000129.3:p.Ser2664Thr
NM_000138.5:c.7990T>A MANE Select	NP_000129.3:p.Ser2664Thr