Canonical Allele Identifier: CA2175508532

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441683T= , CM000677.2:g.48441683T=	GRCh38
NC_000015.9:g.48733880T= , CM000677.1:g.48733880T=	GRCh37
NC_000015.8:g.46521172T=	NCBI36
NG_008805.2:g.209106A= , LRG_778:g.209106A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.6163+38A=	ENSP00000453958.2:n.6163+38A=
ENST00000674301.2:c.6163+38A=	ENSP00000501333.2:n.6163+38A=
ENST00000316623.10:c.6163+38A= MANE Select	ENSP00000325527.5:n.6163+38A=
ENST00000674301.1:c.1162+38A=	ENSP00000501333.1:n.1162+38A=
ENST00000316623.9:c.6163+38A=	ENSP00000325527.5:n.6163+38A=
ENST00000537463.6:c.*1926+38A=	ENSP00000440294.2:n.*1926+38A=
ENST00000559133.5:c.1470+38A=
ENST00000560820.1:n.283+38A=
NM_000138.4:c.6163+38A= , LRG_778t1:c.6163+38A=	NP_000129.3:n.6163+38A=
NM_000138.5:c.6163+38A= MANE Select	NP_000129.3:n.6163+38A=