Canonical Allele Identifier: CA392329931
Community Standard Title: NM_000138.5(FBN1):c.7087T>A (p.Cys2363Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427684A>T , CM000677.2:g.48427684A>T GRCh38
NC_000015.9:g.48719881A>T , CM000677.1:g.48719881A>T GRCh37
NC_000015.8:g.46507173A>T NCBI36
NG_008805.2:g.223105T>A , LRG_778:g.223105T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7087T>A MANE Select NP_000129.3:p.Cys2363Ser
ENST00000316623.10:c.7087T>A MANE Select ENSP00000325527.5:p.Cys2363Ser
NM_000138.4:c.7087T>A , LRG_778t1:c.7087T>A NP_000129.3:p.Cys2363Ser
ENST00000316623.9:c.7087T>A ENSP00000325527.5:p.Cys2363Ser
ENST00000559133.5:c.2456T>A
ENST00000559133.6:c.7149T>A ENSP00000453958.2:p.Asn2383Lys
ENST00000674301.1:c.2253T>A ENSP00000501333.1:n.2253T>A
ENST00000674301.2:c.*600T>A ENSP00000501333.2:n.*600T>A
ENST00000682170.1:n.1268T>A
ENST00000682767.1:n.384T>A