Canonical Allele Identifier: CA2695220421
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537624del , CM000677.2:g.48537624del GRCh38
NC_000015.9:g.48829821del , CM000677.1:g.48829821del GRCh37
NC_000015.8:g.46617113del NCBI36
NG_008805.2:g.113167del , LRG_778:g.113167del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.725del ENSP00000453958.2:p.Gly242GlufsTer?
ENST00000674301.2:c.725del ENSP00000501333.2:p.Gly242GlufsTer?
ENST00000316623.10:c.725del MANE Select ENSP00000325527.5:p.Gly242GlufsTer?
ENST00000316623.9:c.725del ENSP00000325527.5:p.Gly242GlufsTer?
ENST00000537463.6:c.636+89del ENSP00000440294.2:n.636+89del
NM_000138.4:c.725del , LRG_778t1:c.725del NP_000129.3:p.Gly242GlufsTer?
NM_000138.5:c.725del MANE Select NP_000129.3:p.Gly242GlufsTer?