Canonical Allele Identifier: CA2175492079

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472583A= , CM000677.2:g.48472583A=	GRCh38
NC_000015.9:g.48764780A= , CM000677.1:g.48764780A=	GRCh37
NC_000015.8:g.46552072A=	NCBI36
NG_008805.2:g.178206T= , LRG_778:g.178206T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4304T=	ENSP00000453958.2:p.Phe1435=
ENST00000674301.2:c.4304T=	ENSP00000501333.2:p.Phe1435=
ENST00000683268.1:n.271T=
ENST00000684448.1:n.2978T=
ENST00000316623.10:c.4304T= MANE Select	ENSP00000325527.5:p.Phe1435=
ENST00000316623.9:c.4304T=	ENSP00000325527.5:p.Phe1435=
ENST00000537463.6:c.*67T=	ENSP00000440294.2:n.*67T=
NM_000138.4:c.4304T= , LRG_778t1:c.4304T=	NP_000129.3:p.Phe1435=
NM_000138.5:c.4304T= MANE Select	NP_000129.3:p.Phe1435=