Canonical Allele Identifier: CA392322742

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707790T>G (hg19) ; chr15:g.48415593T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415593T>G , CM000677.2:g.48415593T>G	GRCh38
NC_000015.9:g.48707790T>G , CM000677.1:g.48707790T>G	GRCh37
NC_000015.8:g.46495082T>G	NCBI36
NG_008805.2:g.235196A>C , LRG_778:g.235196A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*802A>C	ENSP00000453958.2:n.*802A>C
ENST00000674301.2:c.*1507A>C	ENSP00000501333.2:n.*1507A>C
ENST00000682158.1:n.1375A>C
ENST00000682170.1:n.2175A>C
ENST00000682767.1:n.1291A>C
ENST00000316623.10:c.7994A>C MANE Select	ENSP00000325527.5:p.Asn2665Thr
ENST00000674301.1:c.3160A>C	ENSP00000501333.1:n.3160A>C
ENST00000316623.9:c.7994A>C	ENSP00000325527.5:p.Asn2665Thr
ENST00000559133.5:c.3363A>C
ENST00000561429.1:n.249A>C
NM_000138.4:c.7994A>C , LRG_778t1:c.7994A>C	NP_000129.3:p.Asn2665Thr
NM_000138.5:c.7994A>C MANE Select	NP_000129.3:p.Asn2665Thr