Canonical Allele Identifier: CA2838515738
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48446620dup , CM000677.2:g.48446620dup GRCh38
NC_000015.9:g.48738817dup , CM000677.1:g.48738817dup GRCh37
NC_000015.8:g.46526109dup NCBI36
NG_008805.2:g.204169dup , LRG_778:g.204169dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5788+86dup ENSP00000453958.2:n.5788+86dup
ENST00000674301.2:c.5788+86dup ENSP00000501333.2:n.5788+86dup
ENST00000684448.1:n.4462+86dup
ENST00000316623.10:c.5788+86dup MANE Select ENSP00000325527.5:n.5788+86dup
ENST00000674301.1:c.787+86dup ENSP00000501333.1:n.787+86dup
ENST00000316623.9:c.5788+86dup ENSP00000325527.5:n.5788+86dup
ENST00000537463.6:c.*1551+86dup ENSP00000440294.2:n.*1551+86dup
ENST00000559133.5:c.1095+86dup
NM_000138.4:c.5788+86dup , LRG_778t1:c.5788+86dup NP_000129.3:n.5788+86dup
NM_000138.5:c.5788+86dup MANE Select NP_000129.3:n.5788+86dup