Canonical Allele Identifier: CA2175513370
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445182_48445208delinsATGTATATATATATACATATATATATG , CM000677.2:g.48445182_48445208delinsATGTATATATATATACATATATATATG GRCh38
NC_000015.9:g.48737379_48737405delinsATGTATATATATATACATATATATATG , CM000677.1:g.48737379_48737405delinsATGTATATATATATACATATATATATG GRCh37
NC_000015.8:g.46524671_46524697delinsATGTATATATATATACATATATATATG NCBI36
NG_008805.2:g.205581_205607delinsCATATATATATGTATATATATATACAT , LRG_778:g.205581_205607delinsCATATATATATGTATATATATATACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT ENSP00000453958.2:n.5917+168_5917+194delinsCATATATATATGTATATA...
ENST00000674301.2:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT ENSP00000501333.2:n.5917+168_5917+194delinsCATATATATATGTATATA...
ENST00000684448.1:n.4591+168_4591+194delinsCATATATATATGTATATATATATACAT
ENST00000316623.10:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT MANE Select ENSP00000325527.5:n.5917+168_5917+194delinsCATATATATATGTATATA...
ENST00000674301.1:c.916+168_916+194delinsCATATATATATGTATATATATATACAT ENSP00000501333.1:n.916+168_916+194delinsCATATATATATGTATATATA...
ENST00000316623.9:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT ENSP00000325527.5:n.5917+168_5917+194delinsCATATATATATGTATATA...
ENST00000537463.6:c.*1680+168_*1680+194delinsCATATATATATGTATATATATATACAT ENSP00000440294.2:n.*1680+168_*1680+194delinsCATATATATATGTATA...
ENST00000559133.5:c.1224+168_1224+194delinsCATATATATATGTATATATATATACAT
ENST00000560820.1:n.37+168_37+194delinsCATATATATATGTATATATATATACAT
NM_000138.4:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT , LRG_778t1:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT NP_000129.3:n.5917+168_5917+194delinsCATATATATATGTATATATATATA...
NM_000138.5:c.5917+168_5917+194delinsCATATATATATGTATATATATATACAT MANE Select NP_000129.3:n.5917+168_5917+194delinsCATATATATATGTATATATATATA...