Canonical Allele Identifier: CA2175486902

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411437T= , CM000677.2:g.48411437T=	GRCh38
NC_000015.9:g.48703634T= , CM000677.1:g.48703634T=	GRCh37
NC_000015.8:g.46490926T=	NCBI36
NG_008805.2:g.239352A= , LRG_778:g.239352A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1035-58A=	ENSP00000453958.2:n.*1035-58A=
ENST00000674301.2:c.*1740-58A=	ENSP00000501333.2:n.*1740-58A=
ENST00000682158.1:n.1608-58A=
ENST00000682170.1:n.2408-58A=
ENST00000682767.1:n.1524-58A=
ENST00000316623.10:c.8227-58A= MANE Select	ENSP00000325527.5:n.8227-58A=
ENST00000674301.1:c.3393-58A=	ENSP00000501333.1:n.3393-58A=
ENST00000316623.9:c.8227-58A=	ENSP00000325527.5:n.8227-58A=
ENST00000559133.5:c.3596-58A=
ENST00000561429.1:n.482-58A=
NM_000138.4:c.8227-58A= , LRG_778t1:c.8227-58A=	NP_000129.3:n.8227-58A=
NM_000138.5:c.8227-58A= MANE Select	NP_000129.3:n.8227-58A=