Canonical Allele Identifier: CA392330743
Community Standard Title: NM_000138.5(FBN1):c.6919T>C (p.Cys2307Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428424A>G , CM000677.2:g.48428424A>G GRCh38
NC_000015.9:g.48720621A>G , CM000677.1:g.48720621A>G GRCh37
NC_000015.8:g.46507913A>G NCBI36
NG_008805.2:g.222365T>C , LRG_778:g.222365T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6919T>C MANE Select NP_000129.3:p.Cys2307Arg
ENST00000316623.10:c.6919T>C MANE Select ENSP00000325527.5:p.Cys2307Arg
NM_000138.4:c.6919T>C , LRG_778t1:c.6919T>C NP_000129.3:p.Cys2307Arg
ENST00000316623.9:c.6919T>C ENSP00000325527.5:p.Cys2307Arg
ENST00000559133.5:c.2226T>C
ENST00000559133.6:c.6919T>C ENSP00000453958.2:p.Cys2307Arg
ENST00000560720.1:n.206T>C
ENST00000674301.1:c.2023T>C ENSP00000501333.1:n.2023T>C
ENST00000674301.2:c.*370T>C ENSP00000501333.2:n.*370T>C
ENST00000682170.1:n.528T>C
ENST00000682767.1:n.154T>C