Canonical Allele Identifier: CA1139532474
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2413171
ClinVar RCV Id: RCV003110177

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48503854_48503872del , CM000677.2:g.48503854_48503872del GRCh38
NC_000015.9:g.48796051_48796069del , CM000677.1:g.48796051_48796069del GRCh37
NC_000015.8:g.46583343_46583361del NCBI36
NG_008805.2:g.146923_146941del , LRG_778:g.146923_146941del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2034_2052del ENSP00000453958.2:p.Thr679AlafsTer?
ENST00000674301.2:c.2034_2052del ENSP00000501333.2:p.Thr679AlafsTer?
ENST00000684448.1:n.708_726del
ENST00000316623.10:c.2034_2052del MANE Select ENSP00000325527.5:p.Thr679AlafsTer?
ENST00000316623.9:c.2034_2052del ENSP00000325527.5:p.Thr679AlafsTer?
ENST00000537463.6:c.637-29216_637-29198del ENSP00000440294.2:n.637-29216_637-29198de...
NM_000138.4:c.2034_2052del , LRG_778t1:c.2034_2052del NP_000129.3:p.Thr679AlafsTer?
NM_000138.5:c.2034_2052del MANE Select NP_000129.3:p.Thr679AlafsTer?