Canonical Allele Identifier: CA2509525656
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48432857del , CM000677.2:g.48432857del GRCh38
NC_000015.9:g.48725054del , CM000677.1:g.48725054del GRCh37
NC_000015.8:g.46512346del NCBI36
NG_008805.2:g.217932del , LRG_778:g.217932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6739+9del ENSP00000453958.2:n.6739+9del
ENST00000674301.2:c.*190+9del ENSP00000501333.2:n.*190+9del
ENST00000682170.1:n.348+9del
ENST00000316623.10:c.6739+9del MANE Select ENSP00000325527.5:n.6739+9del
ENST00000674301.1:c.1843+9del ENSP00000501333.1:n.1843+9del
ENST00000316623.9:c.6739+9del ENSP00000325527.5:n.6739+9del
ENST00000537463.6:c.*2502+9del ENSP00000440294.2:n.*2502+9del
ENST00000559133.5:c.2046+9del
ENST00000560720.1:n.26+9del
NM_000138.4:c.6739+9del , LRG_778t1:c.6739+9del NP_000129.3:n.6739+9del
NM_000138.5:c.6739+9del MANE Select NP_000129.3:n.6739+9del