Canonical Allele Identifier: CA392330880

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48720651T>A (hg19) ; chr15:g.48428454T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428454T>A , CM000677.2:g.48428454T>A	GRCh38
NC_000015.9:g.48720651T>A , CM000677.1:g.48720651T>A	GRCh37
NC_000015.8:g.46507943T>A	NCBI36
NG_008805.2:g.222335A>T , LRG_778:g.222335A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6889A>T	ENSP00000453958.2:p.Thr2297Ser
ENST00000674301.2:c.*340A>T	ENSP00000501333.2:n.*340A>T
ENST00000682170.1:n.498A>T
ENST00000682767.1:n.124A>T
ENST00000316623.10:c.6889A>T MANE Select	ENSP00000325527.5:p.Thr2297Ser
ENST00000674301.1:c.1993A>T	ENSP00000501333.1:n.1993A>T
ENST00000316623.9:c.6889A>T	ENSP00000325527.5:p.Thr2297Ser
ENST00000559133.5:c.2196A>T
ENST00000560720.1:n.176A>T
NM_000138.4:c.6889A>T , LRG_778t1:c.6889A>T	NP_000129.3:p.Thr2297Ser
NM_000138.5:c.6889A>T MANE Select	NP_000129.3:p.Thr2297Ser