Canonical Allele Identifier: CA392342467

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2921664
• ClinVar RCV Id: RCV003782686
• COSMIC: COSM962375
• MyVariant Identifiers: chr15:g.48741073C>A (hg19) ; chr15:g.48448876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48448876C>A , CM000677.2:g.48448876C>A	GRCh38
NC_000015.9:g.48741073C>A , CM000677.1:g.48741073C>A	GRCh37
NC_000015.8:g.46528365C>A	NCBI36
NG_008805.2:g.201913G>T , LRG_778:g.201913G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5563G>T	ENSP00000453958.2:p.Glu1855Ter
ENST00000674301.2:c.5563G>T	ENSP00000501333.2:p.Glu1855Ter
ENST00000684448.1:n.4237G>T
ENST00000316623.10:c.5563G>T MANE Select	ENSP00000325527.5:p.Glu1855Ter
ENST00000674301.1:c.562G>T	ENSP00000501333.1:p.Glu188Ter
ENST00000316623.9:c.5563G>T	ENSP00000325527.5:p.Glu1855Ter
ENST00000537463.6:c.*1326G>T	ENSP00000440294.2:n.*1326G>T
ENST00000559133.5:c.870G>T
NM_000138.4:c.5563G>T , LRG_778t1:c.5563G>T	NP_000129.3:p.Glu1855Ter
NM_000138.5:c.5563G>T MANE Select	NP_000129.3:p.Glu1855Ter