Canonical Allele Identifier: CA392317566

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48764765T>G (hg19) ; chr15:g.48472568T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472568T>G , CM000677.2:g.48472568T>G	GRCh38
NC_000015.9:g.48764765T>G , CM000677.1:g.48764765T>G	GRCh37
NC_000015.8:g.46552057T>G	NCBI36
NG_008805.2:g.178221A>C , LRG_778:g.178221A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4319A>C	ENSP00000453958.2:p.Asp1440Ala
ENST00000674301.2:c.4319A>C	ENSP00000501333.2:p.Asp1440Ala
ENST00000683268.1:n.286A>C
ENST00000684448.1:n.2993A>C
ENST00000316623.10:c.4319A>C MANE Select	ENSP00000325527.5:p.Asp1440Ala
ENST00000316623.9:c.4319A>C	ENSP00000325527.5:p.Asp1440Ala
ENST00000537463.6:c.*82A>C	ENSP00000440294.2:n.*82A>C
NM_000138.4:c.4319A>C , LRG_778t1:c.4319A>C	NP_000129.3:p.Asp1440Ala
NM_000138.5:c.4319A>C MANE Select	NP_000129.3:p.Asp1440Ala