Canonical Allele Identifier: CA269522660

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48430791A>G , CM000677.2:g.48430791A>G	GRCh38
NC_000015.9:g.48722988A>G , CM000677.1:g.48722988A>G	GRCh37
NC_000015.8:g.46510280A>G	NCBI36
NG_008805.2:g.219998T>C , LRG_778:g.219998T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.6751T>C MANE Select	NP_000129.3:p.Cys2251Arg
ENST00000316623.10:c.6751T>C MANE Select	ENSP00000325527.5:p.Cys2251Arg
NM_000138.4:c.6751T>C , LRG_778t1:c.6751T>C	NP_000129.3:p.Cys2251Arg
ENST00000316623.9:c.6751T>C	ENSP00000325527.5:p.Cys2251Arg
ENST00000537463.6:c.*2514T>C	ENSP00000440294.2:n.*2514T>C
ENST00000559133.5:c.2058T>C
ENST00000559133.6:c.6751T>C	ENSP00000453958.2:p.Cys2251Arg
ENST00000560720.1:n.38T>C
ENST00000674301.1:c.1855T>C	ENSP00000501333.1:n.1855T>C
ENST00000674301.2:c.*202T>C	ENSP00000501333.2:n.*202T>C
ENST00000682170.1:n.360T>C