Canonical Allele Identifier: CA392334857
Community Standard Title: NM_000138.5(FBN1):c.6575G>A (p.Cys2192Tyr)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48434635C>T , CM000677.2:g.48434635C>T GRCh38
NC_000015.9:g.48726832C>T , CM000677.1:g.48726832C>T GRCh37
NC_000015.8:g.46514124C>T NCBI36
NG_008805.2:g.216154G>A , LRG_778:g.216154G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6575G>A MANE Select NP_000129.3:p.Cys2192Tyr
ENST00000316623.10:c.6575G>A MANE Select ENSP00000325527.5:p.Cys2192Tyr
NM_000138.4:c.6575G>A , LRG_778t1:c.6575G>A NP_000129.3:p.Cys2192Tyr
ENST00000316623.9:c.6575G>A ENSP00000325527.5:p.Cys2192Tyr
ENST00000537463.6:c.*2338G>A ENSP00000440294.2:n.*2338G>A
ENST00000559133.5:c.1882G>A
ENST00000559133.6:c.6575G>A ENSP00000453958.2:p.Cys2192Tyr
ENST00000674301.1:c.1574G>A ENSP00000501333.1:p.Cys525Tyr
ENST00000674301.2:c.6575G>A ENSP00000501333.2:p.Cys2192Tyr
ENST00000682170.1:n.184G>A