Canonical Allele Identifier: CA392336693
Community Standard Title: NM_000138.5(FBN1):c.6391T>C (p.Cys2131Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437066A>G , CM000677.2:g.48437066A>G GRCh38
NC_000015.9:g.48729263A>G , CM000677.1:g.48729263A>G GRCh37
NC_000015.8:g.46516555A>G NCBI36
NG_008805.2:g.213723T>C , LRG_778:g.213723T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6391T>C MANE Select NP_000129.3:p.Cys2131Arg
ENST00000316623.10:c.6391T>C MANE Select ENSP00000325527.5:p.Cys2131Arg
NM_000138.4:c.6391T>C , LRG_778t1:c.6391T>C NP_000129.3:p.Cys2131Arg
ENST00000316623.9:c.6391T>C ENSP00000325527.5:p.Cys2131Arg
ENST00000537463.6:c.*2154T>C ENSP00000440294.2:n.*2154T>C
ENST00000559133.5:c.1698T>C
ENST00000559133.6:c.6391T>C ENSP00000453958.2:p.Cys2131Arg
ENST00000674301.1:c.1390T>C ENSP00000501333.1:p.Cys464Arg
ENST00000674301.2:c.6391T>C ENSP00000501333.2:p.Cys2131Arg