Canonical Allele Identifier: CA392336527

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437006A>G , CM000677.2:g.48437006A>G	GRCh38
NC_000015.9:g.48729203A>G , CM000677.1:g.48729203A>G	GRCh37
NC_000015.8:g.46516495A>G	NCBI36
NG_008805.2:g.213783T>C , LRG_778:g.213783T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.6451T>C MANE Select	NP_000129.3:p.Cys2151Arg
ENST00000316623.10:c.6451T>C MANE Select	ENSP00000325527.5:p.Cys2151Arg
NM_000138.4:c.6451T>C , LRG_778t1:c.6451T>C	NP_000129.3:p.Cys2151Arg
ENST00000316623.9:c.6451T>C	ENSP00000325527.5:p.Cys2151Arg
ENST00000537463.6:c.*2214T>C	ENSP00000440294.2:n.*2214T>C
ENST00000559133.5:c.1758T>C
ENST00000559133.6:c.6451T>C	ENSP00000453958.2:p.Cys2151Arg
ENST00000674301.1:c.1450T>C	ENSP00000501333.1:p.Cys484Arg
ENST00000674301.2:c.6451T>C	ENSP00000501333.2:p.Cys2151Arg
ENST00000682170.1:n.60T>C