Canonical Allele Identifier: CA2175489364
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415600A= , CM000677.2:g.48415600A= GRCh38
NC_000015.9:g.48707797A= , CM000677.1:g.48707797A= GRCh37
NC_000015.8:g.46495089A= NCBI36
NG_008805.2:g.235189T= , LRG_778:g.235189T=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*795T= ENSP00000453958.2:n.*795T=
ENST00000674301.2:c.*1500T= ENSP00000501333.2:n.*1500T=
ENST00000682158.1:n.1368T=
ENST00000682170.1:n.2168T=
ENST00000682767.1:n.1284T=
ENST00000316623.10:c.7987T= MANE Select ENSP00000325527.5:p.Cys2663=
ENST00000674301.1:c.3153T= ENSP00000501333.1:n.3153T=
ENST00000316623.9:c.7987T= ENSP00000325527.5:p.Cys2663=
ENST00000559133.5:c.3356T=
ENST00000561429.1:n.242T=
NM_000138.4:c.7987T= , LRG_778t1:c.7987T= NP_000129.3:p.Cys2663=
NM_000138.5:c.7987T= MANE Select NP_000129.3:p.Cys2663=