Canonical Allele Identifier: CA392324928

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421563C>T , CM000677.2:g.48421563C>T	GRCh38
NC_000015.9:g.48713760C>T , CM000677.1:g.48713760C>T	GRCh37
NC_000015.8:g.46501052C>T	NCBI36
NG_008805.2:g.229226G>A , LRG_778:g.229226G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7694G>A MANE Select	NP_000129.3:p.Cys2565Tyr
ENST00000316623.10:c.7694G>A MANE Select	ENSP00000325527.5:p.Cys2565Tyr
NM_000138.4:c.7694G>A , LRG_778t1:c.7694G>A	NP_000129.3:p.Cys2565Tyr
ENST00000316623.9:c.7694G>A	ENSP00000325527.5:p.Cys2565Tyr
ENST00000559133.5:c.3063G>A
ENST00000559133.6:c.*502G>A	ENSP00000453958.2:n.*502G>A
ENST00000674301.1:c.2860G>A	ENSP00000501333.1:n.2860G>A
ENST00000674301.2:c.*1207G>A	ENSP00000501333.2:n.*1207G>A
ENST00000682170.1:n.1875G>A
ENST00000682767.1:n.991G>A