Canonical Allele Identifier: CA2175488065
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412714C= , CM000677.2:g.48412714C= GRCh38
NC_000015.9:g.48704911C= , CM000677.1:g.48704911C= GRCh37
NC_000015.8:g.46492203C= NCBI36
NG_008805.2:g.238075G= , LRG_778:g.238075G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*889G= ENSP00000453958.2:n.*889G=
ENST00000674301.2:c.*1594G= ENSP00000501333.2:n.*1594G=
ENST00000682158.1:n.1462G=
ENST00000682170.1:n.2262G=
ENST00000682767.1:n.1378G=
ENST00000316623.10:c.8081G= MANE Select ENSP00000325527.5:p.Arg2694=
ENST00000674301.1:c.3247G= ENSP00000501333.1:n.3247G=
ENST00000316623.9:c.8081G= ENSP00000325527.5:p.Arg2694=
ENST00000559133.5:c.3450G=
ENST00000561429.1:n.336G=
NM_000138.4:c.8081G= , LRG_778t1:c.8081G= NP_000129.3:p.Arg2694=
NM_000138.5:c.8081G= MANE Select NP_000129.3:p.Arg2694=