Canonical Allele Identifier: CA013383
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 200156
ClinVar RCV Id: RCV000181659
dbSNP Id: rs794728304

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48494218_48494222del , CM000677.2:g.48494218_48494222del GRCh38
NC_000015.9:g.48786415_48786419del , CM000677.1:g.48786415_48786419del GRCh37
NC_000015.8:g.46573707_46573711del NCBI36
NG_008805.2:g.156569_156573del , LRG_778:g.156569_156573del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2712_2716del ENSP00000453958.2:p.Lys904AsnfsTer4
ENST00000674301.2:c.2712_2716del ENSP00000501333.2:p.Lys904AsnfsTer4
ENST00000684448.1:n.1386_1390del
ENST00000316623.10:c.2712_2716del MANE Select ENSP00000325527.5:p.Lys904AsnfsTer4
ENST00000316623.9:c.2712_2716del ENSP00000325527.5:p.Lys904AsnfsTer4
ENST00000537463.6:c.637-19570_637-19566del ENSP00000440294.2:n.637-19570_637-19566de...
NM_000138.4:c.2712_2716del , LRG_778t1:c.2712_2716del NP_000129.3:p.Lys904AsnfsTer4
NM_000138.5:c.2712_2716del MANE Select NP_000129.3:p.Lys904AsnfsTer4