Canonical Allele Identifier: CA2628329834
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48487029_48487033del , CM000677.2:g.48487029_48487033del GRCh38
NC_000015.9:g.48779226_48779230del , CM000677.1:g.48779226_48779230del GRCh37
NC_000015.8:g.46566518_46566522del NCBI36
NG_008805.2:g.163761_163765del , LRG_778:g.163761_163765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3589+47_3589+51del ENSP00000453958.2:n.3589+47_3589+51del
ENST00000674301.2:c.3589+47_3589+51del ENSP00000501333.2:n.3589+47_3589+51del
ENST00000684448.1:n.2263+47_2263+51del
ENST00000316623.10:c.3589+47_3589+51del MANE Select ENSP00000325527.5:n.3589+47_3589+51del
ENST00000316623.9:c.3589+47_3589+51del ENSP00000325527.5:n.3589+47_3589+51del
ENST00000537463.6:c.637-12378_637-12374del ENSP00000440294.2:n.637-12378_637-12374del
NM_000138.4:c.3589+47_3589+51del , LRG_778t1:c.3589+47_3589+51del NP_000129.3:n.3589+47_3589+51del
NM_000138.5:c.3589+47_3589+51del MANE Select NP_000129.3:n.3589+47_3589+51del