Canonical Allele Identifier: CA392322759

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707794A>G (hg19) ; chr15:g.48415597A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415597A>G , CM000677.2:g.48415597A>G	GRCh38
NC_000015.9:g.48707794A>G , CM000677.1:g.48707794A>G	GRCh37
NC_000015.8:g.46495086A>G	NCBI36
NG_008805.2:g.235192T>C , LRG_778:g.235192T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*798T>C	ENSP00000453958.2:n.*798T>C
ENST00000674301.2:c.*1503T>C	ENSP00000501333.2:n.*1503T>C
ENST00000682158.1:n.1371T>C
ENST00000682170.1:n.2171T>C
ENST00000682767.1:n.1287T>C
ENST00000316623.10:c.7990T>C MANE Select	ENSP00000325527.5:p.Ser2664Pro
ENST00000674301.1:c.3156T>C	ENSP00000501333.1:n.3156T>C
ENST00000316623.9:c.7990T>C	ENSP00000325527.5:p.Ser2664Pro
ENST00000559133.5:c.3359T>C
ENST00000561429.1:n.245T>C
NM_000138.4:c.7990T>C , LRG_778t1:c.7990T>C	NP_000129.3:p.Ser2664Pro
NM_000138.5:c.7990T>C MANE Select	NP_000129.3:p.Ser2664Pro