Canonical Allele Identifier: CA2175489305
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415489T= , CM000677.2:g.48415489T= GRCh38
NC_000015.9:g.48707686T= , CM000677.1:g.48707686T= GRCh37
NC_000015.8:g.46494978T= NCBI36
NG_008805.2:g.235300A= , LRG_778:g.235300A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*859+47A= ENSP00000453958.2:n.*859+47A=
ENST00000674301.2:c.*1564+47A= ENSP00000501333.2:n.*1564+47A=
ENST00000682158.1:n.1432+47A=
ENST00000682170.1:n.2232+47A=
ENST00000682767.1:n.1348+47A=
ENST00000316623.10:c.8051+47A= MANE Select ENSP00000325527.5:n.8051+47A=
ENST00000674301.1:c.3217+47A= ENSP00000501333.1:n.3217+47A=
ENST00000316623.9:c.8051+47A= ENSP00000325527.5:n.8051+47A=
ENST00000559133.5:c.3420+47A=
ENST00000561429.1:n.306+47A=
NM_000138.4:c.8051+47A= , LRG_778t1:c.8051+47A= NP_000129.3:n.8051+47A=
NM_000138.5:c.8051+47A= MANE Select NP_000129.3:n.8051+47A=