Canonical Allele Identifier: CA2175488137

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412882G= , CM000677.2:g.48412882G=	GRCh38
NC_000015.9:g.48705079G= , CM000677.1:g.48705079G=	GRCh37
NC_000015.8:g.46492371G=	NCBI36
NG_008805.2:g.237907C= , LRG_778:g.237907C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*860-139C=	ENSP00000453958.2:n.*860-139C=
ENST00000674301.2:c.*1565-139C=	ENSP00000501333.2:n.*1565-139C=
ENST00000682158.1:n.1433-139C=
ENST00000682170.1:n.2233-139C=
ENST00000682767.1:n.1349-139C=
ENST00000316623.10:c.8052-139C= MANE Select	ENSP00000325527.5:n.8052-139C=
ENST00000674301.1:c.3218-139C=	ENSP00000501333.1:n.3218-139C=
ENST00000316623.9:c.8052-139C=	ENSP00000325527.5:n.8052-139C=
ENST00000559133.5:c.3421-139C=
ENST00000561429.1:n.307-139C=
NM_000138.4:c.8052-139C= , LRG_778t1:c.8052-139C=	NP_000129.3:n.8052-139C=
NM_000138.5:c.8052-139C= MANE Select	NP_000129.3:n.8052-139C=