Canonical Allele Identifier: CA2175495138
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474289C= , CM000677.2:g.48474289C= GRCh38
NC_000015.9:g.48766486C= , CM000677.1:g.48766486C= GRCh37
NC_000015.8:g.46553778C= NCBI36
NG_008805.2:g.176500G= , LRG_778:g.176500G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4176G= ENSP00000453958.2:p.Lys1392=
ENST00000674301.2:c.4176G= ENSP00000501333.2:p.Lys1392=
ENST00000684448.1:n.2850G=
ENST00000316623.10:c.4176G= MANE Select ENSP00000325527.5:p.Lys1392=
ENST00000316623.9:c.4176G= ENSP00000325527.5:p.Lys1392=
ENST00000537463.6:c.848G= ENSP00000440294.2:p.Arg283=
NM_000138.4:c.4176G= , LRG_778t1:c.4176G= NP_000129.3:p.Lys1392=
NM_000138.5:c.4176G= MANE Select NP_000129.3:p.Lys1392=