Canonical Allele Identifier: CA2175502822

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48430769C= , CM000677.2:g.48430769C=	GRCh38
NC_000015.9:g.48722966C= , CM000677.1:g.48722966C=	GRCh37
NC_000015.8:g.46510258C=	NCBI36
NG_008805.2:g.220020G= , LRG_778:g.220020G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.6773G=	ENSP00000453958.2:p.Cys2258=
ENST00000674301.2:c.*224G=	ENSP00000501333.2:n.*224G=
ENST00000682170.1:n.382G=
ENST00000316623.10:c.6773G= MANE Select	ENSP00000325527.5:p.Cys2258=
ENST00000674301.1:c.1877G=	ENSP00000501333.1:n.1877G=
ENST00000316623.9:c.6773G=	ENSP00000325527.5:p.Cys2258=
ENST00000537463.6:c.*2536G=	ENSP00000440294.2:n.*2536G=
ENST00000559133.5:c.2080G=
ENST00000560720.1:n.60G=
NM_000138.4:c.6773G= , LRG_778t1:c.6773G=	NP_000129.3:p.Cys2258=
NM_000138.5:c.6773G= MANE Select	NP_000129.3:p.Cys2258=