Canonical Allele Identifier: CA2628325144
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412456_48412519del , CM000677.2:g.48412456_48412519del GRCh38
NC_000015.9:g.48704653_48704716del , CM000677.1:g.48704653_48704716del GRCh37
NC_000015.8:g.46491945_46492008del NCBI36
NG_008805.2:g.238276_238339del , LRG_778:g.238276_238339del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1034+56_*1034+119del ENSP00000453958.2:n.*1034+56_*1034+119del...
ENST00000674301.2:c.*1739+56_*1739+119del ENSP00000501333.2:n.*1739+56_*1739+119del...
ENST00000682158.1:n.1607+56_1607+119del
ENST00000682170.1:n.2407+56_2407+119del
ENST00000682767.1:n.1523+56_1523+119del
ENST00000316623.10:c.8226+56_8226+119del MANE Select ENSP00000325527.5:n.8226+56_8226+119del
ENST00000674301.1:c.3392+56_3392+119del ENSP00000501333.1:n.3392+56_3392+119del
ENST00000316623.9:c.8226+56_8226+119del ENSP00000325527.5:n.8226+56_8226+119del
ENST00000559133.5:c.3595+56_3595+119del
ENST00000561429.1:n.481+56_481+119del
NM_000138.4:c.8226+56_8226+119del , LRG_778t1:c.8226+56_8226+119del NP_000129.3:n.8226+56_8226+119del
NM_000138.5:c.8226+56_8226+119del MANE Select NP_000129.3:n.8226+56_8226+119del