Canonical Allele Identifier: CA2628347637
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445506_48445507insATACA , CM000677.2:g.48445506_48445507insATACA GRCh38
NC_000015.9:g.48737703_48737704insATACA , CM000677.1:g.48737703_48737704insATACA GRCh37
NC_000015.8:g.46524995_46524996insATACA NCBI36
NG_008805.2:g.205282_205283insTGTAT , LRG_778:g.205282_205283insTGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5789-3_5789-2insTGTAT ENSP00000453958.2:n.5789-3_5789-2insTGTAT
ENST00000674301.2:c.5789-3_5789-2insTGTAT ENSP00000501333.2:n.5789-3_5789-2insTGTAT
ENST00000684448.1:n.4463-3_4463-2insTGTAT
ENST00000316623.10:c.5789-3_5789-2insTGTAT MANE Select ENSP00000325527.5:n.5789-3_5789-2insTGTAT
ENST00000674301.1:c.788-3_788-2insTGTAT ENSP00000501333.1:n.788-3_788-2insTGTAT
ENST00000316623.9:c.5789-3_5789-2insTGTAT ENSP00000325527.5:n.5789-3_5789-2insTGTAT
ENST00000537463.6:c.*1552-3_*1552-2insTGTAT ENSP00000440294.2:n.*1552-3_*1552-2insTGTAT
ENST00000559133.5:c.1096-3_1096-2insTGTAT
NM_000138.4:c.5789-3_5789-2insTGTAT , LRG_778t1:c.5789-3_5789-2insTGTAT NP_000129.3:n.5789-3_5789-2insTGTAT
NM_000138.5:c.5789-3_5789-2insTGTAT MANE Select NP_000129.3:n.5789-3_5789-2insTGTAT