Canonical Allele Identifier: CA2628334071

Gene: FBN1

Linked Data

• gnomAD v4: 15-48472400-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472400_48472401insC , CM000677.2:g.48472400_48472401insC	GRCh38
NC_000015.9:g.48764597_48764598insC , CM000677.1:g.48764597_48764598insC	GRCh37
NC_000015.8:g.46551889_46551890insC	NCBI36
NG_008805.2:g.178388_178389insG , LRG_778:g.178388_178389insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4336+150_4336+151insG	ENSP00000453958.2:n.4336+150_4336+151insG
ENST00000674301.2:c.4336+150_4336+151insG	ENSP00000501333.2:n.4336+150_4336+151insG
ENST00000683268.1:n.303+150_303+151insG
ENST00000684448.1:n.3010+150_3010+151insG
ENST00000316623.10:c.4336+150_4336+151insG MANE Select	ENSP00000325527.5:n.4336+150_4336+151insG
ENST00000316623.9:c.4336+150_4336+151insG	ENSP00000325527.5:n.4336+150_4336+151insG
ENST00000537463.6:c.*99+150_*99+151insG	ENSP00000440294.2:n.*99+150_*99+151insG
NM_000138.4:c.4336+150_4336+151insG , LRG_778t1:c.4336+150_4336+151insG	NP_000129.3:n.4336+150_4336+151insG
NM_000138.5:c.4336+150_4336+151insG MANE Select	NP_000129.3:n.4336+150_4336+151insG