Canonical Allele Identifier: CA2175498386

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428448G= , CM000677.2:g.48428448G=	GRCh38
NC_000015.9:g.48720645G= , CM000677.1:g.48720645G=	GRCh37
NC_000015.8:g.46507937G=	NCBI36
NG_008805.2:g.222341C= , LRG_778:g.222341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6895C=	ENSP00000453958.2:p.Pro2299=
ENST00000674301.2:c.*346C=	ENSP00000501333.2:n.*346C=
ENST00000682170.1:n.504C=
ENST00000682767.1:n.130C=
ENST00000316623.10:c.6895C= MANE Select	ENSP00000325527.5:p.Pro2299=
ENST00000674301.1:c.1999C=	ENSP00000501333.1:n.1999C=
ENST00000316623.9:c.6895C=	ENSP00000325527.5:p.Pro2299=
ENST00000559133.5:c.2202C=
ENST00000560720.1:n.182C=
NM_000138.4:c.6895C= , LRG_778t1:c.6895C=	NP_000129.3:p.Pro2299=
NM_000138.5:c.6895C= MANE Select	NP_000129.3:p.Pro2299=