Canonical Allele Identifier: CA2175489335

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415558C= , CM000677.2:g.48415558C=	GRCh38
NC_000015.9:g.48707755C= , CM000677.1:g.48707755C=	GRCh37
NC_000015.8:g.46495047C=	NCBI36
NG_008805.2:g.235231G= , LRG_778:g.235231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*837G=	ENSP00000453958.2:n.*837G=
ENST00000674301.2:c.*1542G=	ENSP00000501333.2:n.*1542G=
ENST00000682158.1:n.1410G=
ENST00000682170.1:n.2210G=
ENST00000682767.1:n.1326G=
ENST00000316623.10:c.8029G= MANE Select	ENSP00000325527.5:p.Gly2677=
ENST00000674301.1:c.3195G=	ENSP00000501333.1:n.3195G=
ENST00000316623.9:c.8029G=	ENSP00000325527.5:p.Gly2677=
ENST00000559133.5:c.3398G=
ENST00000561429.1:n.284G=
NM_000138.4:c.8029G= , LRG_778t1:c.8029G=	NP_000129.3:p.Gly2677=
NM_000138.5:c.8029G= MANE Select	NP_000129.3:p.Gly2677=