Canonical Allele Identifier: CA392324761
Community Standard Title: NM_000138.5(FBN1):c.7741T>A (p.Cys2581Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48420765A>T , CM000677.2:g.48420765A>T GRCh38
NC_000015.9:g.48712962A>T , CM000677.1:g.48712962A>T GRCh37
NC_000015.8:g.46500254A>T NCBI36
NG_008805.2:g.230024T>A , LRG_778:g.230024T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7741T>A MANE Select NP_000129.3:p.Cys2581Ser
ENST00000316623.10:c.7741T>A MANE Select ENSP00000325527.5:p.Cys2581Ser
NM_000138.4:c.7741T>A , LRG_778t1:c.7741T>A NP_000129.3:p.Cys2581Ser
ENST00000316623.9:c.7741T>A ENSP00000325527.5:p.Cys2581Ser
ENST00000559133.5:c.3110T>A
ENST00000559133.6:c.*549T>A ENSP00000453958.2:n.*549T>A
ENST00000674301.1:c.2907T>A ENSP00000501333.1:n.2907T>A
ENST00000674301.2:c.*1254T>A ENSP00000501333.2:n.*1254T>A
ENST00000682170.1:n.1922T>A
ENST00000682767.1:n.1038T>A