Canonical Allele Identifier: CA2175463922

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421738T= , CM000677.2:g.48421738T=	GRCh38
NC_000015.9:g.48713935T= , CM000677.1:g.48713935T=	GRCh37
NC_000015.8:g.46501227T=	NCBI36
NG_008805.2:g.229051A= , LRG_778:g.229051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*379-52A=	ENSP00000453958.2:n.*379-52A=
ENST00000674301.2:c.*1084-52A=	ENSP00000501333.2:n.*1084-52A=
ENST00000682170.1:n.1752-52A=
ENST00000682767.1:n.868-52A=
ENST00000316623.10:c.7571-52A= MANE Select	ENSP00000325527.5:n.7571-52A=
ENST00000674301.1:c.2737-52A=	ENSP00000501333.1:n.2737-52A=
ENST00000316623.9:c.7571-52A=	ENSP00000325527.5:n.7571-52A=
ENST00000559133.5:c.2940-52A=
NM_000138.4:c.7571-52A= , LRG_778t1:c.7571-52A=	NP_000129.3:n.7571-52A=
NM_000138.5:c.7571-52A= MANE Select	NP_000129.3:n.7571-52A=