Canonical Allele Identifier: CA2175486414
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411171A= , CM000677.2:g.48411171A= GRCh38
NC_000015.9:g.48703368A= , CM000677.1:g.48703368A= GRCh37
NC_000015.8:g.46490660A= NCBI36
NG_008805.2:g.239618T= , LRG_778:g.239618T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1243T= ENSP00000453958.2:n.*1243T=
ENST00000674301.2:c.*1948T= ENSP00000501333.2:n.*1948T=
ENST00000682158.1:n.1816T=
ENST00000682170.1:n.2616T=
ENST00000682767.1:n.1732T=
ENST00000316623.10:c.8435T= MANE Select ENSP00000325527.5:p.Ile2812=
ENST00000674301.1:c.3601T= ENSP00000501333.1:n.3601T=
ENST00000316623.9:c.8435T= ENSP00000325527.5:p.Ile2812=
ENST00000559133.5:c.3804T=
NM_000138.4:c.8435T= , LRG_778t1:c.8435T= NP_000129.3:p.Ile2812=
NM_000138.5:c.8435T= MANE Select NP_000129.3:p.Ile2812=