Canonical Allele Identifier: CA2175492104
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425322C= , CM000677.2:g.48425322C= GRCh38
NC_000015.9:g.48717519C= , CM000677.1:g.48717519C= GRCh37
NC_000015.8:g.46504811C= NCBI36
NG_008805.2:g.225467G= , LRG_778:g.225467G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*261+47G= ENSP00000453958.2:n.*261+47G=
ENST00000674301.2:c.*966+47G= ENSP00000501333.2:n.*966+47G=
ENST00000682170.1:n.1634+47G=
ENST00000682767.1:n.750+47G=
ENST00000316623.10:c.7453+47G= MANE Select ENSP00000325527.5:n.7453+47G=
ENST00000674301.1:c.2619+47G= ENSP00000501333.1:n.2619+47G=
ENST00000316623.9:c.7453+47G= ENSP00000325527.5:n.7453+47G=
ENST00000559133.5:c.2822+47G=
NM_000138.4:c.7453+47G= , LRG_778t1:c.7453+47G= NP_000129.3:n.7453+47G=
NM_000138.5:c.7453+47G= MANE Select NP_000129.3:n.7453+47G=