Canonical Allele Identifier: CA2175497382

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428038T= , CM000677.2:g.48428038T=	GRCh38
NC_000015.9:g.48720235T= , CM000677.1:g.48720235T=	GRCh37
NC_000015.8:g.46507527T=	NCBI36
NG_008805.2:g.222751A= , LRG_778:g.222751A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6998-95A=	ENSP00000453958.2:n.6998-95A=
ENST00000674301.2:c.*449-95A=	ENSP00000501333.2:n.*449-95A=
ENST00000682170.1:n.914A=
ENST00000682767.1:n.233-95A=
ENST00000316623.10:c.6998-265A= MANE Select	ENSP00000325527.5:n.6998-265A=
ENST00000674301.1:c.2102-95A=	ENSP00000501333.1:n.2102-95A=
ENST00000316623.9:c.6998-265A=	ENSP00000325527.5:n.6998-265A=
ENST00000559133.5:c.2305-95A=
ENST00000560720.1:n.592A=
NM_000138.4:c.6998-265A= , LRG_778t1:c.6998-265A=	NP_000129.3:n.6998-265A=
NM_000138.5:c.6998-265A= MANE Select	NP_000129.3:n.6998-265A=