Canonical Allele Identifier: CA392325741
Community Standard Title: NM_000138.5(FBN1):c.7603T>C (p.Cys2535Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421654A>G , CM000677.2:g.48421654A>G GRCh38
NC_000015.9:g.48713851A>G , CM000677.1:g.48713851A>G GRCh37
NC_000015.8:g.46501143A>G NCBI36
NG_008805.2:g.229135T>C , LRG_778:g.229135T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7603T>C MANE Select NP_000129.3:p.Cys2535Arg
ENST00000316623.10:c.7603T>C MANE Select ENSP00000325527.5:p.Cys2535Arg
NM_000138.4:c.7603T>C , LRG_778t1:c.7603T>C NP_000129.3:p.Cys2535Arg
ENST00000316623.9:c.7603T>C ENSP00000325527.5:p.Cys2535Arg
ENST00000559133.5:c.2972T>C
ENST00000559133.6:c.*411T>C ENSP00000453958.2:n.*411T>C
ENST00000674301.1:c.2769T>C ENSP00000501333.1:n.2769T>C
ENST00000674301.2:c.*1116T>C ENSP00000501333.2:n.*1116T>C
ENST00000682170.1:n.1784T>C
ENST00000682767.1:n.900T>C