Canonical Allele Identifier: CA2175492581
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445442C= , CM000677.2:g.48445442C= GRCh38
NC_000015.9:g.48737639C= , CM000677.1:g.48737639C= GRCh37
NC_000015.8:g.46524931C= NCBI36
NG_008805.2:g.205347G= , LRG_778:g.205347G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5851G= ENSP00000453958.2:p.Val1951=
ENST00000674301.2:c.5851G= ENSP00000501333.2:p.Val1951=
ENST00000684448.1:n.4525G=
ENST00000316623.10:c.5851G= MANE Select ENSP00000325527.5:p.Val1951=
ENST00000674301.1:c.850G= ENSP00000501333.1:p.Val284=
ENST00000316623.9:c.5851G= ENSP00000325527.5:p.Val1951=
ENST00000537463.6:c.*1614G= ENSP00000440294.2:n.*1614G=
ENST00000559133.5:c.1158G=
NM_000138.4:c.5851G= , LRG_778t1:c.5851G= NP_000129.3:p.Val1951=
NM_000138.5:c.5851G= MANE Select NP_000129.3:p.Val1951=