Canonical Allele Identifier: CA490016771

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48717636G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425439G>A , CM000677.2:g.48425439G>A	GRCh38
NC_000015.9:g.48717636G>A , CM000677.1:g.48717636G>A	GRCh37
NC_000015.8:g.46504928G>A	NCBI36
NG_008805.2:g.225350C>T , LRG_778:g.225350C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*191C>T	ENSP00000453958.2:n.*191C>T
ENST00000674301.2:c.*896C>T	ENSP00000501333.2:n.*896C>T
ENST00000682170.1:n.1564C>T
ENST00000682767.1:n.680C>T
ENST00000316623.10:c.7383C>T MANE Select	ENSP00000325527.5:p.Asn2461=
ENST00000674301.1:c.2549C>T	ENSP00000501333.1:n.2549C>T
ENST00000316623.9:c.7383C>T	ENSP00000325527.5:p.Asn2461=
ENST00000559133.5:c.2752C>T
NM_000138.4:c.7383C>T , LRG_778t1:c.7383C>T	NP_000129.3:p.Asn2461=
NM_000138.5:c.7383C>T MANE Select	NP_000129.3:p.Asn2461=