Canonical Allele Identifier: CA2695220628
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472689_48472708del , CM000677.2:g.48472689_48472708del GRCh38
NC_000015.9:g.48764886_48764905del , CM000677.1:g.48764886_48764905del GRCh37
NC_000015.8:g.46552178_46552197del NCBI36
NG_008805.2:g.178081_178100del , LRG_778:g.178081_178100del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4211-32_4211-13del ENSP00000453958.2:n.4211-32_4211-13del
ENST00000674301.2:c.4211-32_4211-13del ENSP00000501333.2:n.4211-32_4211-13del
ENST00000683268.1:n.146_165del
ENST00000684448.1:n.2885-32_2885-13del
ENST00000316623.10:c.4211-32_4211-13del MANE Select ENSP00000325527.5:n.4211-32_4211-13del
ENST00000316623.9:c.4211-32_4211-13del ENSP00000325527.5:n.4211-32_4211-13del
ENST00000537463.6:c.883-32_883-13del ENSP00000440294.2:n.883-32_883-13del
NM_000138.4:c.4211-32_4211-13del , LRG_778t1:c.4211-32_4211-13del NP_000129.3:n.4211-32_4211-13del
NM_000138.5:c.4211-32_4211-13del MANE Select NP_000129.3:n.4211-32_4211-13del