Canonical Allele Identifier: CA392319741

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703497G>T (hg19) ; chr15:g.48411300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411300G>T , CM000677.2:g.48411300G>T	GRCh38
NC_000015.9:g.48703497G>T , CM000677.1:g.48703497G>T	GRCh37
NC_000015.8:g.46490789G>T	NCBI36
NG_008805.2:g.239489C>A , LRG_778:g.239489C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1114C>A	ENSP00000453958.2:n.*1114C>A
ENST00000674301.2:c.*1819C>A	ENSP00000501333.2:n.*1819C>A
ENST00000682158.1:n.1687C>A
ENST00000682170.1:n.2487C>A
ENST00000682767.1:n.1603C>A
ENST00000316623.10:c.8306C>A MANE Select	ENSP00000325527.5:p.Ser2769Tyr
ENST00000674301.1:c.3472C>A	ENSP00000501333.1:n.3472C>A
ENST00000316623.9:c.8306C>A	ENSP00000325527.5:p.Ser2769Tyr
ENST00000559133.5:c.3675C>A
ENST00000561429.1:n.561C>A
NM_000138.4:c.8306C>A , LRG_778t1:c.8306C>A	NP_000129.3:p.Ser2769Tyr
NM_000138.5:c.8306C>A MANE Select	NP_000129.3:p.Ser2769Tyr