Canonical Allele Identifier: CA2175521429

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48497377C= , CM000677.2:g.48497377C=	GRCh38
NC_000015.9:g.48789574C= , CM000677.1:g.48789574C=	GRCh37
NC_000015.8:g.46576866C=	NCBI36
NG_008805.2:g.153412G= , LRG_778:g.153412G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.2182G=	ENSP00000453958.2:p.Ala728=
ENST00000674301.2:c.2182G=	ENSP00000501333.2:p.Ala728=
ENST00000684448.1:n.856G=
ENST00000316623.10:c.2182G= MANE Select	ENSP00000325527.5:p.Ala728=
ENST00000316623.9:c.2182G=	ENSP00000325527.5:p.Ala728=
ENST00000537463.6:c.637-22727G=	ENSP00000440294.2:n.637-22727G=
NM_000138.4:c.2182G= , LRG_778t1:c.2182G=	NP_000129.3:p.Ala728=
NM_000138.5:c.2182G= MANE Select	NP_000129.3:p.Ala728=