Canonical Allele Identifier: CA2175497441

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434718_48434720delinsAAG , CM000677.2:g.48434718_48434720delinsAAG	GRCh38
NC_000015.9:g.48726915_48726917delinsAAG , CM000677.1:g.48726915_48726917delinsAAG	GRCh37
NC_000015.8:g.46514207_46514209delinsAAG	NCBI36
NG_008805.2:g.216069_216071delinsCTT , LRG_778:g.216069_216071delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6497-7_6497-5delinsCTT	ENSP00000453958.2:n.6497-7_6497-5delinsCTT
ENST00000674301.2:c.6497-7_6497-5delinsCTT	ENSP00000501333.2:n.6497-7_6497-5delinsCTT
ENST00000682170.1:n.106-7_106-5delinsCTT
ENST00000316623.10:c.6497-7_6497-5delinsCTT MANE Select	ENSP00000325527.5:n.6497-7_6497-5delinsCTT
ENST00000674301.1:c.1496-7_1496-5delinsCTT	ENSP00000501333.1:n.1496-7_1496-5delinsCTT
ENST00000316623.9:c.6497-7_6497-5delinsCTT	ENSP00000325527.5:n.6497-7_6497-5delinsCTT
ENST00000537463.6:c.*2260-7_*2260-5delinsCTT	ENSP00000440294.2:n.*2260-7_*2260-5delinsCTT
ENST00000559133.5:c.1804-7_1804-5delinsCTT
NM_000138.4:c.6497-7_6497-5delinsCTT , LRG_778t1:c.6497-7_6497-5delinsCTT	NP_000129.3:n.6497-7_6497-5delinsCTT
NM_000138.5:c.6497-7_6497-5delinsCTT MANE Select	NP_000129.3:n.6497-7_6497-5delinsCTT