Canonical Allele Identifier: CA392324933
Community Standard Title: NM_000138.5(FBN1):c.7693T>C (p.Cys2565Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421564A>G , CM000677.2:g.48421564A>G GRCh38
NC_000015.9:g.48713761A>G , CM000677.1:g.48713761A>G GRCh37
NC_000015.8:g.46501053A>G NCBI36
NG_008805.2:g.229225T>C , LRG_778:g.229225T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7693T>C MANE Select NP_000129.3:p.Cys2565Arg
ENST00000316623.10:c.7693T>C MANE Select ENSP00000325527.5:p.Cys2565Arg
NM_000138.4:c.7693T>C , LRG_778t1:c.7693T>C NP_000129.3:p.Cys2565Arg
ENST00000316623.9:c.7693T>C ENSP00000325527.5:p.Cys2565Arg
ENST00000559133.5:c.3062T>C
ENST00000559133.6:c.*501T>C ENSP00000453958.2:n.*501T>C
ENST00000674301.1:c.2859T>C ENSP00000501333.1:n.2859T>C
ENST00000674301.2:c.*1206T>C ENSP00000501333.2:n.*1206T>C
ENST00000682170.1:n.1874T>C
ENST00000682767.1:n.990T>C