Canonical Allele Identifier: CA2175486270
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411112T= , CM000677.2:g.48411112T= GRCh38
NC_000015.9:g.48703309T= , CM000677.1:g.48703309T= GRCh37
NC_000015.8:g.46490601T= NCBI36
NG_008805.2:g.239677A= , LRG_778:g.239677A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1302A= ENSP00000453958.2:n.*1302A=
ENST00000674301.2:c.*2007A= ENSP00000501333.2:n.*2007A=
ENST00000682158.1:n.1875A=
ENST00000682170.1:n.2675A=
ENST00000682767.1:n.1791A=
ENST00000316623.10:c.8494A= MANE Select ENSP00000325527.5:p.Ser2832=
ENST00000674301.1:c.3660A= ENSP00000501333.1:n.3660A=
ENST00000316623.9:c.8494A= ENSP00000325527.5:p.Ser2832=
ENST00000559133.5:c.3863A=
NM_000138.4:c.8494A= , LRG_778t1:c.8494A= NP_000129.3:p.Ser2832=
NM_000138.5:c.8494A= MANE Select NP_000129.3:p.Ser2832=