Canonical Allele Identifier: CA2175486648
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411279C= , CM000677.2:g.48411279C= GRCh38
NC_000015.9:g.48703476C= , CM000677.1:g.48703476C= GRCh37
NC_000015.8:g.46490768C= NCBI36
NG_008805.2:g.239510G= , LRG_778:g.239510G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1135G= ENSP00000453958.2:n.*1135G=
ENST00000674301.2:c.*1840G= ENSP00000501333.2:n.*1840G=
ENST00000682158.1:n.1708G=
ENST00000682170.1:n.2508G=
ENST00000682767.1:n.1624G=
ENST00000316623.10:c.8327G= MANE Select ENSP00000325527.5:p.Arg2776=
ENST00000674301.1:c.3493G= ENSP00000501333.1:n.3493G=
ENST00000316623.9:c.8327G= ENSP00000325527.5:p.Arg2776=
ENST00000559133.5:c.3696G=
ENST00000561429.1:n.582G=
NM_000138.4:c.8327G= , LRG_778t1:c.8327G= NP_000129.3:p.Arg2776=
NM_000138.5:c.8327G= MANE Select NP_000129.3:p.Arg2776=