Canonical Allele Identifier: CA392333502

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48725129A>T (hg19) ; chr15:g.48432932A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432932A>T , CM000677.2:g.48432932A>T	GRCh38
NC_000015.9:g.48725129A>T , CM000677.1:g.48725129A>T	GRCh37
NC_000015.8:g.46512421A>T	NCBI36
NG_008805.2:g.217857T>A , LRG_778:g.217857T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6673T>A	ENSP00000453958.2:p.Tyr2225Asn
ENST00000674301.2:c.*124T>A	ENSP00000501333.2:n.*124T>A
ENST00000682170.1:n.282T>A
ENST00000316623.10:c.6673T>A MANE Select	ENSP00000325527.5:p.Tyr2225Asn
ENST00000674301.1:c.1777T>A	ENSP00000501333.1:n.1777T>A
ENST00000316623.9:c.6673T>A	ENSP00000325527.5:p.Tyr2225Asn
ENST00000537463.6:c.*2436T>A	ENSP00000440294.2:n.*2436T>A
ENST00000559133.5:c.1980T>A
NM_000138.4:c.6673T>A , LRG_778t1:c.6673T>A	NP_000129.3:p.Tyr2225Asn
NM_000138.5:c.6673T>A MANE Select	NP_000129.3:p.Tyr2225Asn