Canonical Allele Identifier: CA392322667

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707774G>T (hg19) ; chr15:g.48415577G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415577G>T , CM000677.2:g.48415577G>T	GRCh38
NC_000015.9:g.48707774G>T , CM000677.1:g.48707774G>T	GRCh37
NC_000015.8:g.46495066G>T	NCBI36
NG_008805.2:g.235212C>A , LRG_778:g.235212C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*818C>A	ENSP00000453958.2:n.*818C>A
ENST00000674301.2:c.*1523C>A	ENSP00000501333.2:n.*1523C>A
ENST00000682158.1:n.1391C>A
ENST00000682170.1:n.2191C>A
ENST00000682767.1:n.1307C>A
ENST00000316623.10:c.8010C>A MANE Select	ENSP00000325527.5:p.Tyr2670Ter
ENST00000674301.1:c.3176C>A	ENSP00000501333.1:n.3176C>A
ENST00000316623.9:c.8010C>A	ENSP00000325527.5:p.Tyr2670Ter
ENST00000559133.5:c.3379C>A
ENST00000561429.1:n.265C>A
NM_000138.4:c.8010C>A , LRG_778t1:c.8010C>A	NP_000129.3:p.Tyr2670Ter
NM_000138.5:c.8010C>A MANE Select	NP_000129.3:p.Tyr2670Ter