Canonical Allele Identifier: CA2175486884
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411413T= , CM000677.2:g.48411413T= GRCh38
NC_000015.9:g.48703610T= , CM000677.1:g.48703610T= GRCh37
NC_000015.8:g.46490902T= NCBI36
NG_008805.2:g.239376A= , LRG_778:g.239376A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-34A= ENSP00000453958.2:n.*1035-34A=
ENST00000674301.2:c.*1740-34A= ENSP00000501333.2:n.*1740-34A=
ENST00000682158.1:n.1608-34A=
ENST00000682170.1:n.2408-34A=
ENST00000682767.1:n.1524-34A=
ENST00000316623.10:c.8227-34A= MANE Select ENSP00000325527.5:n.8227-34A=
ENST00000674301.1:c.3393-34A= ENSP00000501333.1:n.3393-34A=
ENST00000316623.9:c.8227-34A= ENSP00000325527.5:n.8227-34A=
ENST00000559133.5:c.3596-34A=
ENST00000561429.1:n.482-34A=
NM_000138.4:c.8227-34A= , LRG_778t1:c.8227-34A= NP_000129.3:n.8227-34A=
NM_000138.5:c.8227-34A= MANE Select NP_000129.3:n.8227-34A=