Canonical Allele Identifier: CA2175495266
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474309_48474310delinsAT , CM000677.2:g.48474309_48474310delinsAT GRCh38
NC_000015.9:g.48766506_48766507delinsAT , CM000677.1:g.48766506_48766507delinsAT GRCh37
NC_000015.8:g.46553798_46553799delinsAT NCBI36
NG_008805.2:g.176479_176480delinsAT , LRG_778:g.176479_176480delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4155_4156delinsAT ENSP00000453958.2:p.Gly1385=
ENST00000674301.2:c.4155_4156delinsAT ENSP00000501333.2:p.Gly1385=
ENST00000684448.1:n.2829_2830delinsAT
ENST00000316623.10:c.4155_4156delinsAT MANE Select ENSP00000325527.5:p.Gly1385=
ENST00000316623.9:c.4155_4156delinsAT ENSP00000325527.5:p.Gly1385=
ENST00000537463.6:c.827_828delinsAT ENSP00000440294.2:p.Asp276=
NM_000138.4:c.4155_4156delinsAT , LRG_778t1:c.4155_4156delinsAT NP_000129.3:p.Gly1385=
NM_000138.5:c.4155_4156delinsAT MANE Select NP_000129.3:p.Gly1385=