Canonical Allele Identifier: CA490016773

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48717639T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425442T>C , CM000677.2:g.48425442T>C	GRCh38
NC_000015.9:g.48717639T>C , CM000677.1:g.48717639T>C	GRCh37
NC_000015.8:g.46504931T>C	NCBI36
NG_008805.2:g.225347A>G , LRG_778:g.225347A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*188A>G	ENSP00000453958.2:n.*188A>G
ENST00000674301.2:c.*893A>G	ENSP00000501333.2:n.*893A>G
ENST00000682170.1:n.1561A>G
ENST00000682767.1:n.677A>G
ENST00000316623.10:c.7380A>G MANE Select	ENSP00000325527.5:p.Lys2460=
ENST00000674301.1:c.2546A>G	ENSP00000501333.1:n.2546A>G
ENST00000316623.9:c.7380A>G	ENSP00000325527.5:p.Lys2460=
ENST00000559133.5:c.2749A>G
NM_000138.4:c.7380A>G , LRG_778t1:c.7380A>G	NP_000129.3:p.Lys2460=
NM_000138.5:c.7380A>G MANE Select	NP_000129.3:p.Lys2460=