Canonical Allele Identifier: CA2175523921

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48492425A= , CM000677.2:g.48492425A=	GRCh38
NC_000015.9:g.48784622A= , CM000677.1:g.48784622A=	GRCh37
NC_000015.8:g.46571914A=	NCBI36
NG_008805.2:g.158364T= , LRG_778:g.158364T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.2854+36T=	ENSP00000453958.2:n.2854+36T=
ENST00000674301.2:c.2854+36T=	ENSP00000501333.2:n.2854+36T=
ENST00000684448.1:n.1528+36T=
ENST00000316623.10:c.2854+36T= MANE Select	ENSP00000325527.5:n.2854+36T=
ENST00000316623.9:c.2854+36T=	ENSP00000325527.5:n.2854+36T=
ENST00000537463.6:c.637-17775T=	ENSP00000440294.2:n.637-17775T=
NM_000138.4:c.2854+36T= , LRG_778t1:c.2854+36T=	NP_000129.3:n.2854+36T=
NM_000138.5:c.2854+36T= MANE Select	NP_000129.3:n.2854+36T=