Canonical Allele Identifier: CA2695220602
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468467dup , CM000677.2:g.48468467dup GRCh38
NC_000015.9:g.48760664dup , CM000677.1:g.48760664dup GRCh37
NC_000015.8:g.46547956dup NCBI36
NG_008805.2:g.182322dup , LRG_778:g.182322dup

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.4527dup ENSP00000453958.2:p.Ile1510TyrfsTer3
ENST00000674301.2:c.4527dup ENSP00000501333.2:p.Ile1510TyrfsTer3
ENST00000684448.1:n.3201dup
ENST00000316623.10:c.4527dup MANE Select ENSP00000325527.5:p.Ile1510TyrfsTer3
ENST00000316623.9:c.4527dup ENSP00000325527.5:p.Ile1510TyrfsTer3
ENST00000537463.6:c.*290dup ENSP00000440294.2:n.*290dup
NM_000138.4:c.4527dup , LRG_778t1:c.4527dup NP_000129.3:p.Ile1510TyrfsTer3
NM_000138.5:c.4527dup MANE Select NP_000129.3:p.Ile1510TyrfsTer3