Canonical Allele Identifier: CA10603851
Community Standard Title: NM_000138.5(FBN1):c.7776C>T (p.Cys2592=)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48420730G>A , CM000677.2:g.48420730G>A GRCh38
NC_000015.9:g.48712927G>A , CM000677.1:g.48712927G>A GRCh37
NC_000015.8:g.46500219G>A NCBI36
NG_008805.2:g.230059C>T , LRG_778:g.230059C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7776C>T MANE Select NP_000129.3:p.Cys2592=
ENST00000316623.10:c.7776C>T MANE Select ENSP00000325527.5:p.Cys2592=
NM_000138.4:c.7776C>T , LRG_778t1:c.7776C>T NP_000129.3:p.Cys2592=
ENST00000316623.9:c.7776C>T ENSP00000325527.5:p.Cys2592=
ENST00000559133.5:c.3145C>T
ENST00000559133.6:c.*584C>T ENSP00000453958.2:n.*584C>T
ENST00000674301.1:c.2942C>T ENSP00000501333.1:n.2942C>T
ENST00000674301.2:c.*1289C>T ENSP00000501333.2:n.*1289C>T
ENST00000682170.1:n.1957C>T
ENST00000682767.1:n.1073C>T