Canonical Allele Identifier: CA2536144325
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410727_48410728insCA , CM000677.2:g.48410727_48410728insCA GRCh38
NC_000015.9:g.48702924_48702925insCA , CM000677.1:g.48702924_48702925insCA GRCh37
NC_000015.8:g.46490216_46490217insCA NCBI36
NG_008805.2:g.240061_240062insTG , LRG_778:g.240061_240062insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1686_*1687insTG ENSP00000453958.2:n.*1686_*1687insTG
ENST00000682158.1:n.2259_2260insTG
ENST00000682170.1:n.3059_3060insTG
ENST00000682767.1:n.2175_2176insTG
ENST00000316623.10:c.*262_*263insTG MANE Select ENSP00000325527.5:n.*262_*263insTG
ENST00000316623.9:c.*262_*263insTG ENSP00000325527.5:n.*262_*263insTG
ENST00000559133.5:c.4247_4248insTG
NM_000138.4:c.*262_*263insTG , LRG_778t1:c.*262_*263insTG NP_000129.3:n.*262_*263insTG
NM_000138.5:c.*262_*263insTG MANE Select NP_000129.3:n.*262_*263insTG