Canonical Allele Identifier: CA2175531430

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48513635C= , CM000677.2:g.48513635C=	GRCh38
NC_000015.9:g.48805832C= , CM000677.1:g.48805832C=	GRCh37
NC_000015.8:g.46593124C=	NCBI36
NG_008805.2:g.137154G= , LRG_778:g.137154G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.1502G=	ENSP00000453958.2:p.Gly501=
ENST00000674301.2:c.1502G=	ENSP00000501333.2:p.Gly501=
ENST00000684448.1:n.176G=
ENST00000316623.10:c.1502G= MANE Select	ENSP00000325527.5:p.Gly501=
ENST00000316623.9:c.1502G=	ENSP00000325527.5:p.Gly501=
ENST00000537463.6:c.636+24076G=	ENSP00000440294.2:n.636+24076G=
NM_000138.4:c.1502G= , LRG_778t1:c.1502G=	NP_000129.3:p.Gly501=
NM_000138.5:c.1502G= MANE Select	NP_000129.3:p.Gly501=