Canonical Allele Identifier: CA2175486118
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411055T= , CM000677.2:g.48411055T= GRCh38
NC_000015.9:g.48703252T= , CM000677.1:g.48703252T= GRCh37
NC_000015.8:g.46490544T= NCBI36
NG_008805.2:g.239734A= , LRG_778:g.239734A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1359A= ENSP00000453958.2:n.*1359A=
ENST00000682158.1:n.1932A=
ENST00000682170.1:n.2732A=
ENST00000682767.1:n.1848A=
ENST00000316623.10:c.8551A= MANE Select ENSP00000325527.5:p.Lys2851=
ENST00000316623.9:c.8551A= ENSP00000325527.5:p.Lys2851=
ENST00000559133.5:c.3920A=
NM_000138.4:c.8551A= , LRG_778t1:c.8551A= NP_000129.3:p.Lys2851=
NM_000138.5:c.8551A= MANE Select NP_000129.3:p.Lys2851=