Canonical Allele Identifier: CA392325838

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48714154C>T (hg19) ; chr15:g.48421957C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421957C>T , CM000677.2:g.48421957C>T	GRCh38
NC_000015.9:g.48714154C>T , CM000677.1:g.48714154C>T	GRCh37
NC_000015.8:g.46501446C>T	NCBI36
NG_008805.2:g.228832G>A , LRG_778:g.228832G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*373G>A	ENSP00000453958.2:n.*373G>A
ENST00000674301.2:c.*1078G>A	ENSP00000501333.2:n.*1078G>A
ENST00000682170.1:n.1746G>A
ENST00000682767.1:n.862G>A
ENST00000316623.10:c.7565G>A MANE Select	ENSP00000325527.5:p.Cys2522Tyr
ENST00000674301.1:c.2731G>A	ENSP00000501333.1:n.2731G>A
ENST00000316623.9:c.7565G>A	ENSP00000325527.5:p.Cys2522Tyr
ENST00000559133.5:c.2934G>A
NM_000138.4:c.7565G>A , LRG_778t1:c.7565G>A	NP_000129.3:p.Cys2522Tyr
NM_000138.5:c.7565G>A MANE Select	NP_000129.3:p.Cys2522Tyr