Canonical Allele Identifier: CA2175486965

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411506G= , CM000677.2:g.48411506G=	GRCh38
NC_000015.9:g.48703703G= , CM000677.1:g.48703703G=	GRCh37
NC_000015.8:g.46490995G=	NCBI36
NG_008805.2:g.239283C= , LRG_778:g.239283C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1035-127C=	ENSP00000453958.2:n.*1035-127C=
ENST00000674301.2:c.*1740-127C=	ENSP00000501333.2:n.*1740-127C=
ENST00000682158.1:n.1608-127C=
ENST00000682170.1:n.2408-127C=
ENST00000682767.1:n.1524-127C=
ENST00000316623.10:c.8227-127C= MANE Select	ENSP00000325527.5:n.8227-127C=
ENST00000674301.1:c.3393-127C=	ENSP00000501333.1:n.3393-127C=
ENST00000316623.9:c.8227-127C=	ENSP00000325527.5:n.8227-127C=
ENST00000559133.5:c.3596-127C=
ENST00000561429.1:n.482-127C=
NM_000138.4:c.8227-127C= , LRG_778t1:c.8227-127C=	NP_000129.3:n.8227-127C=
NM_000138.5:c.8227-127C= MANE Select	NP_000129.3:n.8227-127C=