Canonical Allele Identifier: CA2175529826
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48509971T= , CM000677.2:g.48509971T= GRCh38
NC_000015.9:g.48802168T= , CM000677.1:g.48802168T= GRCh37
NC_000015.8:g.46589460T= NCBI36
NG_008805.2:g.140818A= , LRG_778:g.140818A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1714+73A= ENSP00000453958.2:n.1714+73A=
ENST00000674301.2:c.1714+73A= ENSP00000501333.2:n.1714+73A=
ENST00000684448.1:n.388+73A=
ENST00000316623.10:c.1714+73A= MANE Select ENSP00000325527.5:n.1714+73A=
ENST00000316623.9:c.1714+73A= ENSP00000325527.5:n.1714+73A=
ENST00000537463.6:c.636+27740A= ENSP00000440294.2:n.636+27740A=
NM_000138.4:c.1714+73A= , LRG_778t1:c.1714+73A= NP_000129.3:n.1714+73A=
NM_000138.5:c.1714+73A= MANE Select NP_000129.3:n.1714+73A=