Canonical Allele Identifier: CA2175463932

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421759T= , CM000677.2:g.48421759T=	GRCh38
NC_000015.9:g.48713956T= , CM000677.1:g.48713956T=	GRCh37
NC_000015.8:g.46501248T=	NCBI36
NG_008805.2:g.229030A= , LRG_778:g.229030A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*379-73A=	ENSP00000453958.2:n.*379-73A=
ENST00000674301.2:c.*1084-73A=	ENSP00000501333.2:n.*1084-73A=
ENST00000682170.1:n.1752-73A=
ENST00000682767.1:n.868-73A=
ENST00000316623.10:c.7571-73A= MANE Select	ENSP00000325527.5:n.7571-73A=
ENST00000674301.1:c.2737-73A=	ENSP00000501333.1:n.2737-73A=
ENST00000316623.9:c.7571-73A=	ENSP00000325527.5:n.7571-73A=
ENST00000559133.5:c.2940-73A=
NM_000138.4:c.7571-73A= , LRG_778t1:c.7571-73A=	NP_000129.3:n.7571-73A=
NM_000138.5:c.7571-73A= MANE Select	NP_000129.3:n.7571-73A=