Canonical Allele Identifier: CA2175495047
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474274_48474275delinsAC , CM000677.2:g.48474274_48474275delinsAC GRCh38
NC_000015.9:g.48766471_48766472delinsAC , CM000677.1:g.48766471_48766472delinsAC GRCh37
NC_000015.8:g.46553763_46553764delinsAC NCBI36
NG_008805.2:g.176514_176515delinsGT , LRG_778:g.176514_176515delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4190_4191delinsGT ENSP00000453958.2:p.Gly1397=
ENST00000674301.2:c.4190_4191delinsGT ENSP00000501333.2:p.Gly1397=
ENST00000684448.1:n.2864_2865delinsGT
ENST00000316623.10:c.4190_4191delinsGT MANE Select ENSP00000325527.5:p.Gly1397=
ENST00000316623.9:c.4190_4191delinsGT ENSP00000325527.5:p.Gly1397=
ENST00000537463.6:c.862_863delinsGT ENSP00000440294.2:p.Val288=
NM_000138.4:c.4190_4191delinsGT , LRG_778t1:c.4190_4191delinsGT NP_000129.3:p.Gly1397=
NM_000138.5:c.4190_4191delinsGT MANE Select NP_000129.3:p.Gly1397=