Canonical Allele Identifier: CA2175495065
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474276_48474277delinsCT , CM000677.2:g.48474276_48474277delinsCT GRCh38
NC_000015.9:g.48766473_48766474delinsCT , CM000677.1:g.48766473_48766474delinsCT GRCh37
NC_000015.8:g.46553765_46553766delinsCT NCBI36
NG_008805.2:g.176512_176513delinsAG , LRG_778:g.176512_176513delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4188_4189delinsAG ENSP00000453958.2:p.Thr1396=
ENST00000674301.2:c.4188_4189delinsAG ENSP00000501333.2:p.Thr1396=
ENST00000684448.1:n.2862_2863delinsAG
ENST00000316623.10:c.4188_4189delinsAG MANE Select ENSP00000325527.5:p.Thr1396=
ENST00000316623.9:c.4188_4189delinsAG ENSP00000325527.5:p.Thr1396=
ENST00000537463.6:c.860_861delinsAG ENSP00000440294.2:p.Gln287=
NM_000138.4:c.4188_4189delinsAG , LRG_778t1:c.4188_4189delinsAG NP_000129.3:p.Thr1396=
NM_000138.5:c.4188_4189delinsAG MANE Select NP_000129.3:p.Thr1396=