Canonical Allele Identifier: CA490021385

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441743G>A , CM000677.2:g.48441743G>A	GRCh38
NC_000015.9:g.48733940G>A , CM000677.1:g.48733940G>A	GRCh37
NC_000015.8:g.46521232G>A	NCBI36
NG_008805.2:g.209046C>T , LRG_778:g.209046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6141C>T	ENSP00000453958.2:p.Ser2047=
ENST00000674301.2:c.6141C>T	ENSP00000501333.2:p.Ser2047=
ENST00000316623.10:c.6141C>T MANE Select	ENSP00000325527.5:p.Ser2047=
ENST00000674301.1:c.1140C>T	ENSP00000501333.1:p.Ser380=
ENST00000316623.9:c.6141C>T	ENSP00000325527.5:p.Ser2047=
ENST00000537463.6:c.*1904C>T	ENSP00000440294.2:n.*1904C>T
ENST00000559133.5:c.1448C>T
ENST00000560820.1:n.261C>T
NM_000138.4:c.6141C>T , LRG_778t1:c.6141C>T	NP_000129.3:p.Ser2047=
NM_000138.5:c.6141C>T MANE Select	NP_000129.3:p.Ser2047=