Canonical Allele Identifier: CA269521468

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48427656C>A , CM000677.2:g.48427656C>A	GRCh38
NC_000015.9:g.48719853C>A , CM000677.1:g.48719853C>A	GRCh37
NC_000015.8:g.46507145C>A	NCBI36
NG_008805.2:g.223133G>T , LRG_778:g.223133G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.7177G>T	ENSP00000453958.2:p.Val2393Phe
ENST00000674301.2:c.*628G>T	ENSP00000501333.2:n.*628G>T
ENST00000682170.1:n.1296G>T
ENST00000682767.1:n.412G>T
ENST00000316623.10:c.7115G>T MANE Select	ENSP00000325527.5:p.Gly2372Val
ENST00000674301.1:c.2281G>T	ENSP00000501333.1:n.2281G>T
ENST00000316623.9:c.7115G>T	ENSP00000325527.5:p.Gly2372Val
ENST00000559133.5:c.2484G>T
NM_000138.4:c.7115G>T , LRG_778t1:c.7115G>T	NP_000129.3:p.Gly2372Val
NM_000138.5:c.7115G>T MANE Select	NP_000129.3:p.Gly2372Val