Canonical Allele Identifier: CA2175487821

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412488A= , CM000677.2:g.48412488A=	GRCh38
NC_000015.9:g.48704685A= , CM000677.1:g.48704685A=	GRCh37
NC_000015.8:g.46491977A=	NCBI36
NG_008805.2:g.238301T= , LRG_778:g.238301T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1034+81T=	ENSP00000453958.2:n.*1034+81T=
ENST00000674301.2:c.*1739+81T=	ENSP00000501333.2:n.*1739+81T=
ENST00000682158.1:n.1607+81T=
ENST00000682170.1:n.2407+81T=
ENST00000682767.1:n.1523+81T=
ENST00000316623.10:c.8226+81T= MANE Select	ENSP00000325527.5:n.8226+81T=
ENST00000674301.1:c.3392+81T=	ENSP00000501333.1:n.3392+81T=
ENST00000316623.9:c.8226+81T=	ENSP00000325527.5:n.8226+81T=
ENST00000559133.5:c.3595+81T=
ENST00000561429.1:n.481+81T=
NM_000138.4:c.8226+81T= , LRG_778t1:c.8226+81T=	NP_000129.3:n.8226+81T=
NM_000138.5:c.8226+81T= MANE Select	NP_000129.3:n.8226+81T=