Canonical Allele Identifier: CA2175486793
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411351C= , CM000677.2:g.48411351C= GRCh38
NC_000015.9:g.48703548C= , CM000677.1:g.48703548C= GRCh37
NC_000015.8:g.46490840C= NCBI36
NG_008805.2:g.239438G= , LRG_778:g.239438G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1063G= ENSP00000453958.2:n.*1063G=
ENST00000674301.2:c.*1768G= ENSP00000501333.2:n.*1768G=
ENST00000682158.1:n.1636G=
ENST00000682170.1:n.2436G=
ENST00000682767.1:n.1552G=
ENST00000316623.10:c.8255G= MANE Select ENSP00000325527.5:p.Ser2752=
ENST00000674301.1:c.3421G= ENSP00000501333.1:n.3421G=
ENST00000316623.9:c.8255G= ENSP00000325527.5:p.Ser2752=
ENST00000559133.5:c.3624G=
ENST00000561429.1:n.510G=
NM_000138.4:c.8255G= , LRG_778t1:c.8255G= NP_000129.3:p.Ser2752=
NM_000138.5:c.8255G= MANE Select NP_000129.3:p.Ser2752=