Canonical Allele Identifier: CA392340238

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48737692T>G (hg19) ; chr15:g.48445495T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445495T>G , CM000677.2:g.48445495T>G	GRCh38
NC_000015.9:g.48737692T>G , CM000677.1:g.48737692T>G	GRCh37
NC_000015.8:g.46524984T>G	NCBI36
NG_008805.2:g.205294A>C , LRG_778:g.205294A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5798A>C	ENSP00000453958.2:p.Glu1933Ala
ENST00000674301.2:c.5798A>C	ENSP00000501333.2:p.Glu1933Ala
ENST00000684448.1:n.4472A>C
ENST00000316623.10:c.5798A>C MANE Select	ENSP00000325527.5:p.Glu1933Ala
ENST00000674301.1:c.797A>C	ENSP00000501333.1:p.Glu266Ala
ENST00000316623.9:c.5798A>C	ENSP00000325527.5:p.Glu1933Ala
ENST00000537463.6:c.*1561A>C	ENSP00000440294.2:n.*1561A>C
ENST00000559133.5:c.1105A>C
NM_000138.4:c.5798A>C , LRG_778t1:c.5798A>C	NP_000129.3:p.Glu1933Ala
NM_000138.5:c.5798A>C MANE Select	NP_000129.3:p.Glu1933Ala