Canonical Allele Identifier: CA392326032

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422024A>G , CM000677.2:g.48422024A>G	GRCh38
NC_000015.9:g.48714221A>G , CM000677.1:g.48714221A>G	GRCh37
NC_000015.8:g.46501513A>G	NCBI36
NG_008805.2:g.228765T>C , LRG_778:g.228765T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7498T>C MANE Select	NP_000129.3:p.Cys2500Arg
ENST00000316623.10:c.7498T>C MANE Select	ENSP00000325527.5:p.Cys2500Arg
NM_000138.4:c.7498T>C , LRG_778t1:c.7498T>C	NP_000129.3:p.Cys2500Arg
ENST00000316623.9:c.7498T>C	ENSP00000325527.5:p.Cys2500Arg
ENST00000559133.5:c.2867T>C
ENST00000559133.6:c.*306T>C	ENSP00000453958.2:n.*306T>C
ENST00000674301.1:c.2664T>C	ENSP00000501333.1:n.2664T>C
ENST00000674301.2:c.*1011T>C	ENSP00000501333.2:n.*1011T>C
ENST00000682170.1:n.1679T>C
ENST00000682767.1:n.795T>C