Canonical Allele Identifier: CA2175495124
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474287_48474288delinsTC , CM000677.2:g.48474287_48474288delinsTC GRCh38
NC_000015.9:g.48766484_48766485delinsTC , CM000677.1:g.48766484_48766485delinsTC GRCh37
NC_000015.8:g.46553776_46553777delinsTC NCBI36
NG_008805.2:g.176501_176502delinsGA , LRG_778:g.176501_176502delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4177_4178delinsGA ENSP00000453958.2:p.Glu1393=
ENST00000674301.2:c.4177_4178delinsGA ENSP00000501333.2:p.Glu1393=
ENST00000684448.1:n.2851_2852delinsGA
ENST00000316623.10:c.4177_4178delinsGA MANE Select ENSP00000325527.5:p.Glu1393=
ENST00000316623.9:c.4177_4178delinsGA ENSP00000325527.5:p.Glu1393=
ENST00000537463.6:c.849_850delinsGA ENSP00000440294.2:p.Arg283=
NM_000138.4:c.4177_4178delinsGA , LRG_778t1:c.4177_4178delinsGA NP_000129.3:p.Glu1393=
NM_000138.5:c.4177_4178delinsGA MANE Select NP_000129.3:p.Glu1393=