Canonical Allele Identifier: CA392332198
Community Standard Title: NM_000138.5(FBN1):c.6826T>G (p.Cys2276Gly)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430716A>C , CM000677.2:g.48430716A>C GRCh38
NC_000015.9:g.48722913A>C , CM000677.1:g.48722913A>C GRCh37
NC_000015.8:g.46510205A>C NCBI36
NG_008805.2:g.220073T>G , LRG_778:g.220073T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6826T>G MANE Select NP_000129.3:p.Cys2276Gly
ENST00000316623.10:c.6826T>G MANE Select ENSP00000325527.5:p.Cys2276Gly
NM_000138.4:c.6826T>G , LRG_778t1:c.6826T>G NP_000129.3:p.Cys2276Gly
ENST00000316623.9:c.6826T>G ENSP00000325527.5:p.Cys2276Gly
ENST00000559133.5:c.2133T>G
ENST00000559133.6:c.6826T>G ENSP00000453958.2:p.Cys2276Gly
ENST00000560720.1:n.113T>G
ENST00000674301.1:c.1930T>G ENSP00000501333.1:n.1930T>G
ENST00000674301.2:c.*277T>G ENSP00000501333.2:n.*277T>G
ENST00000682170.1:n.435T>G