Canonical Allele Identifier: CA392337018

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437828A>C , CM000677.2:g.48437828A>C	GRCh38
NC_000015.9:g.48730025A>C , CM000677.1:g.48730025A>C	GRCh37
NC_000015.8:g.46517317A>C	NCBI36
NG_008805.2:g.212961T>G , LRG_778:g.212961T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.6253T>G MANE Select	NP_000129.3:p.Cys2085Gly
ENST00000316623.10:c.6253T>G MANE Select	ENSP00000325527.5:p.Cys2085Gly
NM_000138.4:c.6253T>G , LRG_778t1:c.6253T>G	NP_000129.3:p.Cys2085Gly
ENST00000316623.9:c.6253T>G	ENSP00000325527.5:p.Cys2085Gly
ENST00000537463.6:c.*2016T>G	ENSP00000440294.2:n.*2016T>G
ENST00000559133.5:c.1560T>G
ENST00000559133.6:c.6253T>G	ENSP00000453958.2:p.Cys2085Gly
ENST00000560820.1:n.373T>G
ENST00000674301.1:c.1252T>G	ENSP00000501333.1:p.Cys418Gly
ENST00000674301.2:c.6253T>G	ENSP00000501333.2:p.Cys2085Gly