Canonical Allele Identifier: CA2175492501
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445430G= , CM000677.2:g.48445430G= GRCh38
NC_000015.9:g.48737627G= , CM000677.1:g.48737627G= GRCh37
NC_000015.8:g.46524919G= NCBI36
NG_008805.2:g.205359C= , LRG_778:g.205359C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5863C= ENSP00000453958.2:p.Gln1955=
ENST00000674301.2:c.5863C= ENSP00000501333.2:p.Gln1955=
ENST00000684448.1:n.4537C=
ENST00000316623.10:c.5863C= MANE Select ENSP00000325527.5:p.Gln1955=
ENST00000674301.1:c.862C= ENSP00000501333.1:p.Gln288=
ENST00000316623.9:c.5863C= ENSP00000325527.5:p.Gln1955=
ENST00000537463.6:c.*1626C= ENSP00000440294.2:n.*1626C=
ENST00000559133.5:c.1170C=
NM_000138.4:c.5863C= , LRG_778t1:c.5863C= NP_000129.3:p.Gln1955=
NM_000138.5:c.5863C= MANE Select NP_000129.3:p.Gln1955=