Canonical Allele Identifier: CA2175498105

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48448761T= , CM000677.2:g.48448761T=	GRCh38
NC_000015.9:g.48740958T= , CM000677.1:g.48740958T=	GRCh37
NC_000015.8:g.46528250T=	NCBI36
NG_008805.2:g.202028A= , LRG_778:g.202028A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.5671+7A=	ENSP00000453958.2:n.5671+7A=
ENST00000674301.2:c.5671+7A=	ENSP00000501333.2:n.5671+7A=
ENST00000684448.1:n.4345+7A=
ENST00000316623.10:c.5671+7A= MANE Select	ENSP00000325527.5:n.5671+7A=
ENST00000674301.1:c.670+7A=	ENSP00000501333.1:n.670+7A=
ENST00000316623.9:c.5671+7A=	ENSP00000325527.5:n.5671+7A=
ENST00000537463.6:c.*1434+7A=	ENSP00000440294.2:n.*1434+7A=
ENST00000559133.5:c.978+7A=
NM_000138.4:c.5671+7A= , LRG_778t1:c.5671+7A=	NP_000129.3:n.5671+7A=
NM_000138.5:c.5671+7A= MANE Select	NP_000129.3:n.5671+7A=