Canonical Allele Identifier: CA392325136
Community Standard Title: NM_000138.5(FBN1):c.7648T>A (p.Cys2550Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421609A>T , CM000677.2:g.48421609A>T GRCh38
NC_000015.9:g.48713806A>T , CM000677.1:g.48713806A>T GRCh37
NC_000015.8:g.46501098A>T NCBI36
NG_008805.2:g.229180T>A , LRG_778:g.229180T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7648T>A MANE Select NP_000129.3:p.Cys2550Ser
ENST00000316623.10:c.7648T>A MANE Select ENSP00000325527.5:p.Cys2550Ser
NM_000138.4:c.7648T>A , LRG_778t1:c.7648T>A NP_000129.3:p.Cys2550Ser
ENST00000316623.9:c.7648T>A ENSP00000325527.5:p.Cys2550Ser
ENST00000559133.5:c.3017T>A
ENST00000559133.6:c.*456T>A ENSP00000453958.2:n.*456T>A
ENST00000674301.1:c.2814T>A ENSP00000501333.1:n.2814T>A
ENST00000674301.2:c.*1161T>A ENSP00000501333.2:n.*1161T>A
ENST00000682170.1:n.1829T>A
ENST00000682767.1:n.945T>A