Canonical Allele Identifier: CA2804070434
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445648_48445649insGCTATGAGGTGGCTCCAGATGGGAGGACCTGTGTGGGTAAGTACAGGACTTAGAA , CM000677.2:g.48445648_48445649insGCTATGAGGTGGCTCCAGATGGGAGGACCTGTGTGGGTAAGTACAGGACTTAGAA GRCh38
NC_000015.9:g.48737845_48737846insGCTATGAGGTGGCTCCAGATGGGAGGACCTGTGTGGGTAAGTACAGGACTTAGAA , CM000677.1:g.48737845_48737846insGCTATGAGGTGGCTCCAGATGGGAGGACCTGTGTGGGTAAGTACAGGACTTAGAA GRCh37
NC_000015.8:g.46525137_46525138insGCTATGAGGTGGCTCCAGATGGGAGGACCTGTGTGGGTAAGTACAGGACTTAGAA NCBI36
NG_008805.2:g.205140_205141insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC , LRG_778:g.205140_205141insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC ENSP00000453958.2:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCC...
ENST00000674301.2:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC ENSP00000501333.2:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCC...
ENST00000684448.1:n.4463-145_4463-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC
ENST00000316623.10:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC MANE Select ENSP00000325527.5:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCC...
ENST00000674301.1:c.788-145_788-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC ENSP00000501333.1:n.788-145_788-144insTTCTAAGTCCTGTACTTACCCAC...
ENST00000316623.9:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC ENSP00000325527.5:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCC...
ENST00000537463.6:c.*1552-145_*1552-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC ENSP00000440294.2:n.*1552-145_*1552-144insTTCTAAGTCCTGTACTTAC...
ENST00000559133.5:c.1096-145_1096-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC
NM_000138.4:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC , LRG_778t1:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC NP_000129.3:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAG...
NM_000138.5:c.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAGGTCCTCCCATCTGGAGCCACCTCATAGC MANE Select NP_000129.3:n.5789-145_5789-144insTTCTAAGTCCTGTACTTACCCACACAG...