Canonical Allele Identifier: CA392320897

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48704819T>C (hg19) ; chr15:g.48412622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412622T>C , CM000677.2:g.48412622T>C	GRCh38
NC_000015.9:g.48704819T>C , CM000677.1:g.48704819T>C	GRCh37
NC_000015.8:g.46492111T>C	NCBI36
NG_008805.2:g.238167A>G , LRG_778:g.238167A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*981A>G	ENSP00000453958.2:n.*981A>G
ENST00000674301.2:c.*1686A>G	ENSP00000501333.2:n.*1686A>G
ENST00000682158.1:n.1554A>G
ENST00000682170.1:n.2354A>G
ENST00000682767.1:n.1470A>G
ENST00000316623.10:c.8173A>G MANE Select	ENSP00000325527.5:p.Lys2725Glu
ENST00000674301.1:c.3339A>G	ENSP00000501333.1:n.3339A>G
ENST00000316623.9:c.8173A>G	ENSP00000325527.5:p.Lys2725Glu
ENST00000559133.5:c.3542A>G
ENST00000561429.1:n.428A>G
NM_000138.4:c.8173A>G , LRG_778t1:c.8173A>G	NP_000129.3:p.Lys2725Glu
NM_000138.5:c.8173A>G MANE Select	NP_000129.3:p.Lys2725Glu