Canonical Allele Identifier: CA353638
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222623
ClinVar RCV Id: RCV000208150
dbSNP Id: rs869025424

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425811del , CM000677.2:g.48425811del GRCh38
NC_000015.9:g.48718008del , CM000677.1:g.48718008del GRCh37
NC_000015.8:g.46505300del NCBI36
NG_008805.2:g.224979del , LRG_778:g.224979del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*67del ENSP00000453958.2:n.*67del
ENST00000674301.2:c.*772del ENSP00000501333.2:n.*772del
ENST00000682170.1:n.1440del
ENST00000682767.1:n.556del
ENST00000316623.10:c.7259del MANE Select ENSP00000325527.5:p.Asn2420MetfsTer18
ENST00000674301.1:c.2425del ENSP00000501333.1:n.2425del
ENST00000316623.9:c.7259del ENSP00000325527.5:p.Asn2420MetfsTer18
ENST00000559133.5:c.2628del
NM_000138.4:c.7259del , LRG_778t1:c.7259del NP_000129.3:p.Asn2420MetfsTer18
NM_000138.5:c.7259del MANE Select NP_000129.3:p.Asn2420MetfsTer18