Canonical Allele Identifier: CA392325905
Community Standard Title: NM_000138.5(FBN1):c.7533T>G (p.Cys2511Trp)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421989A>C , CM000677.2:g.48421989A>C GRCh38
NC_000015.9:g.48714186A>C , CM000677.1:g.48714186A>C GRCh37
NC_000015.8:g.46501478A>C NCBI36
NG_008805.2:g.228800T>G , LRG_778:g.228800T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7533T>G MANE Select NP_000129.3:p.Cys2511Trp
ENST00000316623.10:c.7533T>G MANE Select ENSP00000325527.5:p.Cys2511Trp
NM_000138.4:c.7533T>G , LRG_778t1:c.7533T>G NP_000129.3:p.Cys2511Trp
ENST00000316623.9:c.7533T>G ENSP00000325527.5:p.Cys2511Trp
ENST00000559133.5:c.2902T>G
ENST00000559133.6:c.*341T>G ENSP00000453958.2:n.*341T>G
ENST00000674301.1:c.2699T>G ENSP00000501333.1:n.2699T>G
ENST00000674301.2:c.*1046T>G ENSP00000501333.2:n.*1046T>G
ENST00000682170.1:n.1714T>G
ENST00000682767.1:n.830T>G