Canonical Allele Identifier: CA2628325327

Gene: FBN1

Linked Data

• gnomAD v4: 15-48412744-C-CCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412744_48412745insCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT , CM000677.2:g.48412744_48412745insCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT	GRCh38
NC_000015.9:g.48704941_48704942insCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT , CM000677.1:g.48704941_48704942insCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT	GRCh37
NC_000015.8:g.46492233_46492234insCTTGGCCTATGCGGAAGTAACCAGGTGGACAGCCACACAGGTAACCGCCCTCGGTAT	NCBI36
NG_008805.2:g.238044_238045insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG , LRG_778:g.238044_238045insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*860-2_*860-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG	ENSP00000453958.2:n.*860-2_*860-1insATACCGAGGGCGGTTACCTGTGTGG...
ENST00000674301.2:c.*1565-2_*1565-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG	ENSP00000501333.2:n.*1565-2_*1565-1insATACCGAGGGCGGTTACCTGTGT...
ENST00000682158.1:n.1433-2_1433-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG
ENST00000682170.1:n.2233-2_2233-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG
ENST00000682767.1:n.1349-2_1349-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG
ENST00000316623.10:c.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG MANE Select	ENSP00000325527.5:n.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGG...
ENST00000674301.1:c.3218-2_3218-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG	ENSP00000501333.1:n.3218-2_3218-1insATACCGAGGGCGGTTACCTGTGTGG...
ENST00000316623.9:c.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG	ENSP00000325527.5:n.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGG...
ENST00000559133.5:c.3421-2_3421-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG
ENST00000561429.1:n.307-2_307-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG
NM_000138.4:c.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG , LRG_778t1:c.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG	NP_000129.3:n.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCC...
NM_000138.5:c.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCCACCTGGTTACTTCCGCATAGGCCAAG MANE Select	NP_000129.3:n.8052-2_8052-1insATACCGAGGGCGGTTACCTGTGTGGCTGTCC...