Canonical Allele Identifier: CA2628325047

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411393-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411393T>G , CM000677.2:g.48411393T>G	GRCh38
NC_000015.9:g.48703590T>G , CM000677.1:g.48703590T>G	GRCh37
NC_000015.8:g.46490882T>G	NCBI36
NG_008805.2:g.239396A>C , LRG_778:g.239396A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1035-14A>C	ENSP00000453958.2:n.*1035-14A>C
ENST00000674301.2:c.*1740-14A>C	ENSP00000501333.2:n.*1740-14A>C
ENST00000682158.1:n.1608-14A>C
ENST00000682170.1:n.2408-14A>C
ENST00000682767.1:n.1524-14A>C
ENST00000316623.10:c.8227-14A>C MANE Select	ENSP00000325527.5:n.8227-14A>C
ENST00000674301.1:c.3393-14A>C	ENSP00000501333.1:n.3393-14A>C
ENST00000316623.9:c.8227-14A>C	ENSP00000325527.5:n.8227-14A>C
ENST00000559133.5:c.3596-14A>C
ENST00000561429.1:n.482-14A>C
NM_000138.4:c.8227-14A>C , LRG_778t1:c.8227-14A>C	NP_000129.3:n.8227-14A>C
NM_000138.5:c.8227-14A>C MANE Select	NP_000129.3:n.8227-14A>C