Canonical Allele Identifier: CA1139663888
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 933201
ClinVar RCV Id: RCV001201278
dbSNP Id: rs2043402071
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474310del , CM000677.2:g.48474310del GRCh38
NC_000015.9:g.48766507del , CM000677.1:g.48766507del GRCh37
NC_000015.8:g.46553799del NCBI36
NG_008805.2:g.176479del , LRG_778:g.176479del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4155del ENSP00000453958.2:p.Ser1386LeufsTer27
ENST00000674301.2:c.4155del ENSP00000501333.2:p.Ser1386LeufsTer27
ENST00000684448.1:n.2829del
ENST00000316623.10:c.4155del MANE Select ENSP00000325527.5:p.Ser1386LeufsTer27
ENST00000316623.9:c.4155del ENSP00000325527.5:p.Ser1386LeufsTer27
ENST00000537463.6:c.827del ENSP00000440294.2:p.Asp276ValfsTer13
NM_000138.4:c.4155del , LRG_778t1:c.4155del NP_000129.3:p.Ser1386LeufsTer27
NM_000138.5:c.4155del MANE Select NP_000129.3:p.Ser1386LeufsTer27
Search 100 bp 5'
Search 100 bp 3'