Canonical Allele Identifier: CA16602234
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1073641
ClinVar RCV Id: RCV001386704
dbSNP Id: rs2141280222
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474596del , CM000677.2:g.48474596del GRCh38
NC_000015.9:g.48766793del , CM000677.1:g.48766793del GRCh37
NC_000015.8:g.46554085del NCBI36
NG_008805.2:g.176194del , LRG_778:g.176194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4020del ENSP00000453958.2:p.Asn1341IlefsTer?
ENST00000674301.2:c.4020del ENSP00000501333.2:p.Asn1341IlefsTer?
ENST00000684448.1:n.2694del
ENST00000316623.10:c.4020del MANE Select ENSP00000325527.5:p.Asn1341IlefsTer?
ENST00000316623.9:c.4020del ENSP00000325527.5:p.Asn1341IlefsTer?
ENST00000537463.6:c.692del ENSP00000440294.2:p.Pro231GlnfsTer9
NM_000138.4:c.4020del , LRG_778t1:c.4020del NP_000129.3:p.Asn1341IlefsTer?
NM_000138.5:c.4020del MANE Select NP_000129.3:p.Asn1341IlefsTer?
Search 100 bp 5'
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