Canonical Allele Identifier: CA392332601

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48722955G>T (hg19) ; chr15:g.48430758G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48430758G>T , CM000677.2:g.48430758G>T	GRCh38
NC_000015.9:g.48722955G>T , CM000677.1:g.48722955G>T	GRCh37
NC_000015.8:g.46510247G>T	NCBI36
NG_008805.2:g.220031C>A , LRG_778:g.220031C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.6784C>A	ENSP00000453958.2:p.Gln2262Lys
ENST00000674301.2:c.*235C>A	ENSP00000501333.2:n.*235C>A
ENST00000682170.1:n.393C>A
ENST00000316623.10:c.6784C>A MANE Select	ENSP00000325527.5:p.Gln2262Lys
ENST00000674301.1:c.1888C>A	ENSP00000501333.1:n.1888C>A
ENST00000316623.9:c.6784C>A	ENSP00000325527.5:p.Gln2262Lys
ENST00000559133.5:c.2091C>A
ENST00000560720.1:n.71C>A
NM_000138.4:c.6784C>A , LRG_778t1:c.6784C>A	NP_000129.3:p.Gln2262Lys
NM_000138.5:c.6784C>A MANE Select	NP_000129.3:p.Gln2262Lys