Canonical Allele Identifier: CA2175497889

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428337T= , CM000677.2:g.48428337T=	GRCh38
NC_000015.9:g.48720534T= , CM000677.1:g.48720534T=	GRCh37
NC_000015.8:g.46507826T=	NCBI36
NG_008805.2:g.222452A= , LRG_778:g.222452A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6997+9A=	ENSP00000453958.2:n.6997+9A=
ENST00000674301.2:c.*448+9A=	ENSP00000501333.2:n.*448+9A=
ENST00000682170.1:n.615A=
ENST00000682767.1:n.232+9A=
ENST00000316623.10:c.6997+9A= MANE Select	ENSP00000325527.5:n.6997+9A=
ENST00000674301.1:c.2101+9A=	ENSP00000501333.1:n.2101+9A=
ENST00000316623.9:c.6997+9A=	ENSP00000325527.5:n.6997+9A=
ENST00000559133.5:c.2304+9A=
ENST00000560720.1:n.293A=
NM_000138.4:c.6997+9A= , LRG_778t1:c.6997+9A=	NP_000129.3:n.6997+9A=
NM_000138.5:c.6997+9A= MANE Select	NP_000129.3:n.6997+9A=