Canonical Allele Identifier: CA2628334269

Gene: FBN1

Linked Data

• gnomAD v4: 15-48472477-A-AGC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472477_48472478insGC , CM000677.2:g.48472477_48472478insGC	GRCh38
NC_000015.9:g.48764674_48764675insGC , CM000677.1:g.48764674_48764675insGC	GRCh37
NC_000015.8:g.46551966_46551967insGC	NCBI36
NG_008805.2:g.178311_178312insGC , LRG_778:g.178311_178312insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4336+73_4336+74insGC	ENSP00000453958.2:n.4336+73_4336+74insGC
ENST00000674301.2:c.4336+73_4336+74insGC	ENSP00000501333.2:n.4336+73_4336+74insGC
ENST00000683268.1:n.303+73_303+74insGC
ENST00000684448.1:n.3010+73_3010+74insGC
ENST00000316623.10:c.4336+73_4336+74insGC MANE Select	ENSP00000325527.5:n.4336+73_4336+74insGC
ENST00000316623.9:c.4336+73_4336+74insGC	ENSP00000325527.5:n.4336+73_4336+74insGC
ENST00000537463.6:c.*99+73_*99+74insGC	ENSP00000440294.2:n.*99+73_*99+74insGC
NM_000138.4:c.4336+73_4336+74insGC , LRG_778t1:c.4336+73_4336+74insGC	NP_000129.3:n.4336+73_4336+74insGC
NM_000138.5:c.4336+73_4336+74insGC MANE Select	NP_000129.3:n.4336+73_4336+74insGC