Canonical Allele Identifier: CA392327661

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48717590G>T (hg19) ; chr15:g.48425393G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425393G>T , CM000677.2:g.48425393G>T	GRCh38
NC_000015.9:g.48717590G>T , CM000677.1:g.48717590G>T	GRCh37
NC_000015.8:g.46504882G>T	NCBI36
NG_008805.2:g.225396C>A , LRG_778:g.225396C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*237C>A	ENSP00000453958.2:n.*237C>A
ENST00000674301.2:c.*942C>A	ENSP00000501333.2:n.*942C>A
ENST00000682170.1:n.1610C>A
ENST00000682767.1:n.726C>A
ENST00000316623.10:c.7429C>A MANE Select	ENSP00000325527.5:p.Gln2477Lys
ENST00000674301.1:c.2595C>A	ENSP00000501333.1:n.2595C>A
ENST00000316623.9:c.7429C>A	ENSP00000325527.5:p.Gln2477Lys
ENST00000559133.5:c.2798C>A
NM_000138.4:c.7429C>A , LRG_778t1:c.7429C>A	NP_000129.3:p.Gln2477Lys
NM_000138.5:c.7429C>A MANE Select	NP_000129.3:p.Gln2477Lys