Canonical Allele Identifier: CA2575716982
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448927del , CM000677.2:g.48448927del GRCh38
NC_000015.9:g.48741124del , CM000677.1:g.48741124del GRCh37
NC_000015.8:g.46528416del NCBI36
NG_008805.2:g.201862del , LRG_778:g.201862del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5546-34del ENSP00000453958.2:n.5546-34del
ENST00000674301.2:c.5546-34del ENSP00000501333.2:n.5546-34del
ENST00000684448.1:n.4220-34del
ENST00000316623.10:c.5546-34del MANE Select ENSP00000325527.5:n.5546-34del
ENST00000674301.1:c.545-34del ENSP00000501333.1:n.545-34del
ENST00000316623.9:c.5546-34del ENSP00000325527.5:n.5546-34del
ENST00000537463.6:c.*1309-34del ENSP00000440294.2:n.*1309-34del
ENST00000559133.5:c.853-34del
NM_000138.4:c.5546-34del , LRG_778t1:c.5546-34del NP_000129.3:n.5546-34del
NM_000138.5:c.5546-34del MANE Select NP_000129.3:n.5546-34del