Canonical Allele Identifier: CA2175508359

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441547A= , CM000677.2:g.48441547A=	GRCh38
NC_000015.9:g.48733744A= , CM000677.1:g.48733744A=	GRCh37
NC_000015.8:g.46521036A=	NCBI36
NG_008805.2:g.209242T= , LRG_778:g.209242T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6163+174T=	ENSP00000453958.2:n.6163+174T=
ENST00000674301.2:c.6163+174T=	ENSP00000501333.2:n.6163+174T=
ENST00000316623.10:c.6163+174T= MANE Select	ENSP00000325527.5:n.6163+174T=
ENST00000674301.1:c.1162+174T=	ENSP00000501333.1:n.1162+174T=
ENST00000316623.9:c.6163+174T=	ENSP00000325527.5:n.6163+174T=
ENST00000537463.6:c.*1926+174T=	ENSP00000440294.2:n.*1926+174T=
ENST00000559133.5:c.1470+174T=
ENST00000560820.1:n.283+174T=
NM_000138.4:c.6163+174T= , LRG_778t1:c.6163+174T=	NP_000129.3:n.6163+174T=
NM_000138.5:c.6163+174T= MANE Select	NP_000129.3:n.6163+174T=