Canonical Allele Identifier: CA2175495274
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474310_48474311delinsTC , CM000677.2:g.48474310_48474311delinsTC GRCh38
NC_000015.9:g.48766507_48766508delinsTC , CM000677.1:g.48766507_48766508delinsTC GRCh37
NC_000015.8:g.46553799_46553800delinsTC NCBI36
NG_008805.2:g.176478_176479delinsGA , LRG_778:g.176478_176479delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4154_4155delinsGA ENSP00000453958.2:p.Gly1385=
ENST00000674301.2:c.4154_4155delinsGA ENSP00000501333.2:p.Gly1385=
ENST00000684448.1:n.2828_2829delinsGA
ENST00000316623.10:c.4154_4155delinsGA MANE Select ENSP00000325527.5:p.Gly1385=
ENST00000316623.9:c.4154_4155delinsGA ENSP00000325527.5:p.Gly1385=
ENST00000537463.6:c.826_827delinsGA ENSP00000440294.2:p.Asp276=
NM_000138.4:c.4154_4155delinsGA , LRG_778t1:c.4154_4155delinsGA NP_000129.3:p.Gly1385=
NM_000138.5:c.4154_4155delinsGA MANE Select NP_000129.3:p.Gly1385=