Canonical Allele Identifier: CA2175495082

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446755G= , CM000677.2:g.48446755G=	GRCh38
NC_000015.9:g.48738952G= , CM000677.1:g.48738952G=	GRCh37
NC_000015.8:g.46526244G=	NCBI36
NG_008805.2:g.204034C= , LRG_778:g.204034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5739C=	ENSP00000453958.2:p.Asn1913=
ENST00000674301.2:c.5739C=	ENSP00000501333.2:p.Asn1913=
ENST00000684448.1:n.4413C=
ENST00000316623.10:c.5739C= MANE Select	ENSP00000325527.5:p.Asn1913=
ENST00000674301.1:c.738C=	ENSP00000501333.1:p.Asn246=
ENST00000316623.9:c.5739C=	ENSP00000325527.5:p.Asn1913=
ENST00000537463.6:c.*1502C=	ENSP00000440294.2:n.*1502C=
ENST00000559133.5:c.1046C=
NM_000138.4:c.5739C= , LRG_778t1:c.5739C=	NP_000129.3:p.Asn1913=
NM_000138.5:c.5739C= MANE Select	NP_000129.3:p.Asn1913=