Canonical Allele Identifier: CA392326831
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48487436A>T , CM000677.2:g.48487436A>T GRCh38
NC_000015.9:g.48779633A>T , CM000677.1:g.48779633A>T GRCh37
NC_000015.8:g.46566925A>T NCBI36
NG_008805.2:g.163353T>A , LRG_778:g.163353T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3339T>A ENSP00000453958.2:p.Asp1113Glu
ENST00000674301.2:c.3339T>A ENSP00000501333.2:p.Asp1113Glu
ENST00000684448.1:n.2013T>A
ENST00000316623.10:c.3339T>A MANE Select ENSP00000325527.5:p.Asp1113Glu
ENST00000316623.9:c.3339T>A ENSP00000325527.5:p.Asp1113Glu
ENST00000537463.6:c.637-12786T>A ENSP00000440294.2:n.637-12786T>A
NM_000138.4:c.3339T>A , LRG_778t1:c.3339T>A NP_000129.3:p.Asp1113Glu
NM_000138.5:c.3339T>A MANE Select NP_000129.3:p.Asp1113Glu