Canonical Allele Identifier: CA2175516182
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48463957G= , CM000677.2:g.48463957G= GRCh38
NC_000015.9:g.48756154G= , CM000677.1:g.48756154G= GRCh37
NC_000015.8:g.46543446G= NCBI36
NG_008805.2:g.186832C= , LRG_778:g.186832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5007C= ENSP00000453958.2:p.Asn1669=
ENST00000674301.2:c.5007C= ENSP00000501333.2:p.Asn1669=
ENST00000684448.1:n.3681C=
ENST00000316623.10:c.5007C= MANE Select ENSP00000325527.5:p.Asn1669=
ENST00000674301.1:c.6C= ENSP00000501333.1:p.Asn2=
ENST00000316623.9:c.5007C= ENSP00000325527.5:p.Asn1669=
ENST00000537463.6:c.*770C= ENSP00000440294.2:n.*770C=
ENST00000559133.5:c.314C=
NM_000138.4:c.5007C= , LRG_778t1:c.5007C= NP_000129.3:p.Asn1669=
NM_000138.5:c.5007C= MANE Select NP_000129.3:p.Asn1669=