Canonical Allele Identifier: CA2175489425
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415699T= , CM000677.2:g.48415699T= GRCh38
NC_000015.9:g.48707896T= , CM000677.1:g.48707896T= GRCh37
NC_000015.8:g.46495188T= NCBI36
NG_008805.2:g.235090A= , LRG_778:g.235090A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*696A= ENSP00000453958.2:n.*696A=
ENST00000674301.2:c.*1401A= ENSP00000501333.2:n.*1401A=
ENST00000682158.1:n.1269A=
ENST00000682170.1:n.2069A=
ENST00000682767.1:n.1185A=
ENST00000316623.10:c.7888A= MANE Select ENSP00000325527.5:p.Lys2630=
ENST00000674301.1:c.3054A= ENSP00000501333.1:n.3054A=
ENST00000316623.9:c.7888A= ENSP00000325527.5:p.Lys2630=
ENST00000559133.5:c.3257A=
ENST00000561429.1:n.143A=
NM_000138.4:c.7888A= , LRG_778t1:c.7888A= NP_000129.3:p.Lys2630=
NM_000138.5:c.7888A= MANE Select NP_000129.3:p.Lys2630=