Canonical Allele Identifier: CA490023017

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48738994G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446797G>T , CM000677.2:g.48446797G>T	GRCh38
NC_000015.9:g.48738994G>T , CM000677.1:g.48738994G>T	GRCh37
NC_000015.8:g.46526286G>T	NCBI36
NG_008805.2:g.203992C>A , LRG_778:g.203992C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5697C>A	ENSP00000453958.2:p.Ala1899=
ENST00000674301.2:c.5697C>A	ENSP00000501333.2:p.Ala1899=
ENST00000684448.1:n.4371C>A
ENST00000316623.10:c.5697C>A MANE Select	ENSP00000325527.5:p.Ala1899=
ENST00000674301.1:c.696C>A	ENSP00000501333.1:p.Ala232=
ENST00000316623.9:c.5697C>A	ENSP00000325527.5:p.Ala1899=
ENST00000537463.6:c.*1460C>A	ENSP00000440294.2:n.*1460C>A
ENST00000559133.5:c.1004C>A
NM_000138.4:c.5697C>A , LRG_778t1:c.5697C>A	NP_000129.3:p.Ala1899=
NM_000138.5:c.5697C>A MANE Select	NP_000129.3:p.Ala1899=