Canonical Allele Identifier: CA392320697

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48704774T>A (hg19) ; chr15:g.48412577T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412577T>A , CM000677.2:g.48412577T>A	GRCh38
NC_000015.9:g.48704774T>A , CM000677.1:g.48704774T>A	GRCh37
NC_000015.8:g.46492066T>A	NCBI36
NG_008805.2:g.238212A>T , LRG_778:g.238212A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*1026A>T	ENSP00000453958.2:n.*1026A>T
ENST00000674301.2:c.*1731A>T	ENSP00000501333.2:n.*1731A>T
ENST00000682158.1:n.1599A>T
ENST00000682170.1:n.2399A>T
ENST00000682767.1:n.1515A>T
ENST00000316623.10:c.8218A>T MANE Select	ENSP00000325527.5:p.Asn2740Tyr
ENST00000674301.1:c.3384A>T	ENSP00000501333.1:n.3384A>T
ENST00000316623.9:c.8218A>T	ENSP00000325527.5:p.Asn2740Tyr
ENST00000559133.5:c.3587A>T
ENST00000561429.1:n.473A>T
NM_000138.4:c.8218A>T , LRG_778t1:c.8218A>T	NP_000129.3:p.Asn2740Tyr
NM_000138.5:c.8218A>T MANE Select	NP_000129.3:p.Asn2740Tyr