Canonical Allele Identifier: CA2175495685

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446885C= , CM000677.2:g.48446885C=	GRCh38
NC_000015.9:g.48739082C= , CM000677.1:g.48739082C=	GRCh37
NC_000015.8:g.46526374C=	NCBI36
NG_008805.2:g.203904G= , LRG_778:g.203904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5672-63G=	ENSP00000453958.2:n.5672-63G=
ENST00000674301.2:c.5672-63G=	ENSP00000501333.2:n.5672-63G=
ENST00000684448.1:n.4346-63G=
ENST00000316623.10:c.5672-63G= MANE Select	ENSP00000325527.5:n.5672-63G=
ENST00000674301.1:c.671-63G=	ENSP00000501333.1:n.671-63G=
ENST00000316623.9:c.5672-63G=	ENSP00000325527.5:n.5672-63G=
ENST00000537463.6:c.*1435-63G=	ENSP00000440294.2:n.*1435-63G=
ENST00000559133.5:c.979-63G=
NM_000138.4:c.5672-63G= , LRG_778t1:c.5672-63G=	NP_000129.3:n.5672-63G=
NM_000138.5:c.5672-63G= MANE Select	NP_000129.3:n.5672-63G=