Canonical Allele Identifier: CA392319079

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703373T>G (hg19) ; chr15:g.48411176T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411176T>G , CM000677.2:g.48411176T>G	GRCh38
NC_000015.9:g.48703373T>G , CM000677.1:g.48703373T>G	GRCh37
NC_000015.8:g.46490665T>G	NCBI36
NG_008805.2:g.239613A>C , LRG_778:g.239613A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1238A>C	ENSP00000453958.2:n.*1238A>C
ENST00000674301.2:c.*1943A>C	ENSP00000501333.2:n.*1943A>C
ENST00000682158.1:n.1811A>C
ENST00000682170.1:n.2611A>C
ENST00000682767.1:n.1727A>C
ENST00000316623.10:c.8430A>C MANE Select	ENSP00000325527.5:p.Glu2810Asp
ENST00000674301.1:c.3596A>C	ENSP00000501333.1:n.3596A>C
ENST00000316623.9:c.8430A>C	ENSP00000325527.5:p.Glu2810Asp
ENST00000559133.5:c.3799A>C
NM_000138.4:c.8430A>C , LRG_778t1:c.8430A>C	NP_000129.3:p.Glu2810Asp
NM_000138.5:c.8430A>C MANE Select	NP_000129.3:p.Glu2810Asp