Canonical Allele Identifier: CA2695220639
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474569dup , CM000677.2:g.48474569dup GRCh38
NC_000015.9:g.48766766dup , CM000677.1:g.48766766dup GRCh37
NC_000015.8:g.46554058dup NCBI36
NG_008805.2:g.176220dup , LRG_778:g.176220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4046dup ENSP00000453958.2:p.Ser1349ArgfsTer12
ENST00000674301.2:c.4046dup ENSP00000501333.2:p.Ser1349ArgfsTer12
ENST00000684448.1:n.2720dup
ENST00000316623.10:c.4046dup MANE Select ENSP00000325527.5:p.Ser1349ArgfsTer12
ENST00000316623.9:c.4046dup ENSP00000325527.5:p.Ser1349ArgfsTer12
ENST00000537463.6:c.718dup ENSP00000440294.2:p.Ala240GlyfsTer?
NM_000138.4:c.4046dup , LRG_778t1:c.4046dup NP_000129.3:p.Ser1349ArgfsTer12
NM_000138.5:c.4046dup MANE Select NP_000129.3:p.Ser1349ArgfsTer12
Search 100 bp 5'
Search 100 bp 3'