Canonical Allele Identifier: CA2175464830
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48422090G= , CM000677.2:g.48422090G= GRCh38
NC_000015.9:g.48714287G= , CM000677.1:g.48714287G= GRCh37
NC_000015.8:g.46501579G= NCBI36
NG_008805.2:g.228699C= , LRG_778:g.228699C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*262-22C= ENSP00000453958.2:n.*262-22C=
ENST00000674301.2:c.*967-22C= ENSP00000501333.2:n.*967-22C=
ENST00000682170.1:n.1635-22C=
ENST00000682767.1:n.751-22C=
ENST00000316623.10:c.7454-22C= MANE Select ENSP00000325527.5:n.7454-22C=
ENST00000674301.1:c.2620-22C= ENSP00000501333.1:n.2620-22C=
ENST00000316623.9:c.7454-22C= ENSP00000325527.5:n.7454-22C=
ENST00000559133.5:c.2823-22C=
NM_000138.4:c.7454-22C= , LRG_778t1:c.7454-22C= NP_000129.3:n.7454-22C=
NM_000138.5:c.7454-22C= MANE Select NP_000129.3:n.7454-22C=