Canonical Allele Identifier: CA2175486246
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411104A= , CM000677.2:g.48411104A= GRCh38
NC_000015.9:g.48703301A= , CM000677.1:g.48703301A= GRCh37
NC_000015.8:g.46490593A= NCBI36
NG_008805.2:g.239685T= , LRG_778:g.239685T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1310T= ENSP00000453958.2:n.*1310T=
ENST00000674301.2:c.*2015T= ENSP00000501333.2:n.*2015T=
ENST00000682158.1:n.1883T=
ENST00000682170.1:n.2683T=
ENST00000682767.1:n.1799T=
ENST00000316623.10:c.8502T= MANE Select ENSP00000325527.5:p.Thr2834=
ENST00000674301.1:c.3668T= ENSP00000501333.1:n.3668T=
ENST00000316623.9:c.8502T= ENSP00000325527.5:p.Thr2834=
ENST00000559133.5:c.3871T=
NM_000138.4:c.8502T= , LRG_778t1:c.8502T= NP_000129.3:p.Thr2834=
NM_000138.5:c.8502T= MANE Select NP_000129.3:p.Thr2834=