Canonical Allele Identifier: CA2175488142

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412900C= , CM000677.2:g.48412900C=	GRCh38
NC_000015.9:g.48705097C= , CM000677.1:g.48705097C=	GRCh37
NC_000015.8:g.46492389C=	NCBI36
NG_008805.2:g.237889G= , LRG_778:g.237889G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*860-157G=	ENSP00000453958.2:n.*860-157G=
ENST00000674301.2:c.*1565-157G=	ENSP00000501333.2:n.*1565-157G=
ENST00000682158.1:n.1433-157G=
ENST00000682170.1:n.2233-157G=
ENST00000682767.1:n.1349-157G=
ENST00000316623.10:c.8052-157G= MANE Select	ENSP00000325527.5:n.8052-157G=
ENST00000674301.1:c.3218-157G=	ENSP00000501333.1:n.3218-157G=
ENST00000316623.9:c.8052-157G=	ENSP00000325527.5:n.8052-157G=
ENST00000559133.5:c.3421-157G=
ENST00000561429.1:n.307-157G=
NM_000138.4:c.8052-157G= , LRG_778t1:c.8052-157G=	NP_000129.3:n.8052-157G=
NM_000138.5:c.8052-157G= MANE Select	NP_000129.3:n.8052-157G=