Canonical Allele Identifier: CA2175511965
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48444557T= , CM000677.2:g.48444557T= GRCh38
NC_000015.9:g.48736754T= , CM000677.1:g.48736754T= GRCh37
NC_000015.8:g.46524046T= NCBI36
NG_008805.2:g.206232A= , LRG_778:g.206232A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6021A= ENSP00000453958.2:p.Gln2007=
ENST00000674301.2:c.6021A= ENSP00000501333.2:p.Gln2007=
ENST00000684448.1:n.4695A=
ENST00000316623.10:c.6021A= MANE Select ENSP00000325527.5:p.Gln2007=
ENST00000674301.1:c.1020A= ENSP00000501333.1:p.Gln340=
ENST00000316623.9:c.6021A= ENSP00000325527.5:p.Gln2007=
ENST00000537463.6:c.*1784A= ENSP00000440294.2:n.*1784A=
ENST00000559133.5:c.1328A=
ENST00000560820.1:n.141A=
NM_000138.4:c.6021A= , LRG_778t1:c.6021A= NP_000129.3:p.Gln2007=
NM_000138.5:c.6021A= MANE Select NP_000129.3:p.Gln2007=