Canonical Allele Identifier: CA2175502078

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48436961C= , CM000677.2:g.48436961C=	GRCh38
NC_000015.9:g.48729158C= , CM000677.1:g.48729158C=	GRCh37
NC_000015.8:g.46516450C=	NCBI36
NG_008805.2:g.213828G= , LRG_778:g.213828G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.6496G= MANE Select	NP_000129.3:p.Asp2166=
ENST00000316623.10:c.6496G= MANE Select	ENSP00000325527.5:p.Asp2166=
NM_000138.4:c.6496G= , LRG_778t1:c.6496G=	NP_000129.3:p.Asp2166=
ENST00000316623.9:c.6496G=	ENSP00000325527.5:p.Asp2166=
ENST00000537463.6:c.*2259G=	ENSP00000440294.2:n.*2259G=
ENST00000559133.5:c.1803G=
ENST00000559133.6:c.6496G=	ENSP00000453958.2:p.Asp2166=
ENST00000674301.1:c.1495G=	ENSP00000501333.1:p.Asp499=
ENST00000674301.2:c.6496G=	ENSP00000501333.2:p.Asp2166=
ENST00000682170.1:n.105G=