Canonical Allele Identifier: CA2573150825
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678122
ClinVar RCV Id: RCV002224713
dbSNP Id: rs2141357984

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537621_48537639dup , CM000677.2:g.48537621_48537639dup GRCh38
NC_000015.9:g.48829818_48829836dup , CM000677.1:g.48829818_48829836dup GRCh37
NC_000015.8:g.46617110_46617128dup NCBI36
NG_008805.2:g.113150_113168dup , LRG_778:g.113150_113168dup

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.708_726dup ENSP00000453958.2:p.Ala243SerfsTer13
ENST00000674301.2:c.708_726dup ENSP00000501333.2:p.Ala243SerfsTer13
ENST00000316623.10:c.708_726dup MANE Select ENSP00000325527.5:p.Ala243SerfsTer13
ENST00000316623.9:c.708_726dup ENSP00000325527.5:p.Ala243SerfsTer13
ENST00000537463.6:c.636+72_636+90dup ENSP00000440294.2:n.636+72_636+90dup
NM_000138.4:c.708_726dup , LRG_778t1:c.708_726dup NP_000129.3:p.Ala243SerfsTer13
NM_000138.5:c.708_726dup MANE Select NP_000129.3:p.Ala243SerfsTer13