Canonical Allele Identifier: CA490016779

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48717645G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425448G>A , CM000677.2:g.48425448G>A	GRCh38
NC_000015.9:g.48717645G>A , CM000677.1:g.48717645G>A	GRCh37
NC_000015.8:g.46504937G>A	NCBI36
NG_008805.2:g.225341C>T , LRG_778:g.225341C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*182C>T	ENSP00000453958.2:n.*182C>T
ENST00000674301.2:c.*887C>T	ENSP00000501333.2:n.*887C>T
ENST00000682170.1:n.1555C>T
ENST00000682767.1:n.671C>T
ENST00000316623.10:c.7374C>T MANE Select	ENSP00000325527.5:p.Ile2458=
ENST00000674301.1:c.2540C>T	ENSP00000501333.1:n.2540C>T
ENST00000316623.9:c.7374C>T	ENSP00000325527.5:p.Ile2458=
ENST00000559133.5:c.2743C>T
NM_000138.4:c.7374C>T , LRG_778t1:c.7374C>T	NP_000129.3:p.Ile2458=
NM_000138.5:c.7374C>T MANE Select	NP_000129.3:p.Ile2458=