Canonical Allele Identifier: CA2695220641
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474612del , CM000677.2:g.48474612del GRCh38
NC_000015.9:g.48766809del , CM000677.1:g.48766809del GRCh37
NC_000015.8:g.46554101del NCBI36
NG_008805.2:g.176179del , LRG_778:g.176179del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4005del ENSP00000453958.2:p.Lys1335AsnfsTer?
ENST00000674301.2:c.4005del ENSP00000501333.2:p.Lys1335AsnfsTer?
ENST00000684448.1:n.2679del
ENST00000316623.10:c.4005del MANE Select ENSP00000325527.5:p.Lys1335AsnfsTer?
ENST00000316623.9:c.4005del ENSP00000325527.5:p.Lys1335AsnfsTer?
ENST00000537463.6:c.677del ENSP00000440294.2:p.Asn226ThrfsTer14
NM_000138.4:c.4005del , LRG_778t1:c.4005del NP_000129.3:p.Lys1335AsnfsTer?
NM_000138.5:c.4005del MANE Select NP_000129.3:p.Lys1335AsnfsTer?