Canonical Allele Identifier: CA2175464013
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421811T= , CM000677.2:g.48421811T= GRCh38
NC_000015.9:g.48714008T= , CM000677.1:g.48714008T= GRCh37
NC_000015.8:g.46501300T= NCBI36
NG_008805.2:g.228978A= , LRG_778:g.228978A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-125A= ENSP00000453958.2:n.*379-125A=
ENST00000674301.2:c.*1084-125A= ENSP00000501333.2:n.*1084-125A=
ENST00000682170.1:n.1752-125A=
ENST00000682767.1:n.868-125A=
ENST00000316623.10:c.7571-125A= MANE Select ENSP00000325527.5:n.7571-125A=
ENST00000674301.1:c.2737-125A= ENSP00000501333.1:n.2737-125A=
ENST00000316623.9:c.7571-125A= ENSP00000325527.5:n.7571-125A=
ENST00000559133.5:c.2940-125A=
NM_000138.4:c.7571-125A= , LRG_778t1:c.7571-125A= NP_000129.3:n.7571-125A=
NM_000138.5:c.7571-125A= MANE Select NP_000129.3:n.7571-125A=