Canonical Allele Identifier: CA2175498410
Community Standard Title: NM_000138.5(FBN1):c.5595C= (p.Cys1865=)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448844G= , CM000677.2:g.48448844G= GRCh38
NC_000015.9:g.48741041G= , CM000677.1:g.48741041G= GRCh37
NC_000015.8:g.46528333G= NCBI36
NG_008805.2:g.201945C= , LRG_778:g.201945C=

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5595C= MANE Select NP_000129.3:p.Cys1865=
ENST00000316623.10:c.5595C= MANE Select ENSP00000325527.5:p.Cys1865=
NM_000138.4:c.5595C= , LRG_778t1:c.5595C= NP_000129.3:p.Cys1865=
ENST00000316623.9:c.5595C= ENSP00000325527.5:p.Cys1865=
ENST00000537463.6:c.*1358C= ENSP00000440294.2:n.*1358C=
ENST00000559133.5:c.902C=
ENST00000559133.6:c.5595C= ENSP00000453958.2:p.Cys1865=
ENST00000674301.1:c.594C= ENSP00000501333.1:p.Cys198=
ENST00000674301.2:c.5595C= ENSP00000501333.2:p.Cys1865=
ENST00000684448.1:n.4269C=