Canonical Allele Identifier: CA2175503664

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437779G= , CM000677.2:g.48437779G=	GRCh38
NC_000015.9:g.48729976G= , CM000677.1:g.48729976G=	GRCh37
NC_000015.8:g.46517268G=	NCBI36
NG_008805.2:g.213010C= , LRG_778:g.213010C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6302C=	ENSP00000453958.2:p.Thr2101=
ENST00000674301.2:c.6302C=	ENSP00000501333.2:p.Thr2101=
ENST00000316623.10:c.6302C= MANE Select	ENSP00000325527.5:p.Thr2101=
ENST00000674301.1:c.1301C=	ENSP00000501333.1:p.Thr434=
ENST00000316623.9:c.6302C=	ENSP00000325527.5:p.Thr2101=
ENST00000537463.6:c.*2065C=	ENSP00000440294.2:n.*2065C=
ENST00000559133.5:c.1609C=
ENST00000560820.1:n.422C=
NM_000138.4:c.6302C= , LRG_778t1:c.6302C=	NP_000129.3:p.Thr2101=
NM_000138.5:c.6302C= MANE Select	NP_000129.3:p.Thr2101=