Canonical Allele Identifier: CA2175509096

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441820C= , CM000677.2:g.48441820C=	GRCh38
NC_000015.9:g.48734017C= , CM000677.1:g.48734017C=	GRCh37
NC_000015.8:g.46521309C=	NCBI36
NG_008805.2:g.208969G= , LRG_778:g.208969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6064G=	ENSP00000453958.2:p.Glu2022=
ENST00000674301.2:c.6064G=	ENSP00000501333.2:p.Glu2022=
ENST00000316623.10:c.6064G= MANE Select	ENSP00000325527.5:p.Glu2022=
ENST00000674301.1:c.1063G=	ENSP00000501333.1:p.Glu355=
ENST00000316623.9:c.6064G=	ENSP00000325527.5:p.Glu2022=
ENST00000537463.6:c.*1827G=	ENSP00000440294.2:n.*1827G=
ENST00000559133.5:c.1371G=
ENST00000560820.1:n.184G=
NM_000138.4:c.6064G= , LRG_778t1:c.6064G=	NP_000129.3:p.Glu2022=
NM_000138.5:c.6064G= MANE Select	NP_000129.3:p.Glu2022=