Canonical Allele Identifier: CA490015868

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48714192G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421995G>A , CM000677.2:g.48421995G>A	GRCh38
NC_000015.9:g.48714192G>A , CM000677.1:g.48714192G>A	GRCh37
NC_000015.8:g.46501484G>A	NCBI36
NG_008805.2:g.228794C>T , LRG_778:g.228794C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*335C>T	ENSP00000453958.2:n.*335C>T
ENST00000674301.2:c.*1040C>T	ENSP00000501333.2:n.*1040C>T
ENST00000682170.1:n.1708C>T
ENST00000682767.1:n.824C>T
ENST00000316623.10:c.7527C>T MANE Select	ENSP00000325527.5:p.Cys2509=
ENST00000674301.1:c.2693C>T	ENSP00000501333.1:n.2693C>T
ENST00000316623.9:c.7527C>T	ENSP00000325527.5:p.Cys2509=
ENST00000559133.5:c.2896C>T
NM_000138.4:c.7527C>T , LRG_778t1:c.7527C>T	NP_000129.3:p.Cys2509=
NM_000138.5:c.7527C>T MANE Select	NP_000129.3:p.Cys2509=