Canonical Allele Identifier: CA392339838

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48736827T>A (hg19) ; chr15:g.48444630T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48444630T>A , CM000677.2:g.48444630T>A	GRCh38
NC_000015.9:g.48736827T>A , CM000677.1:g.48736827T>A	GRCh37
NC_000015.8:g.46524119T>A	NCBI36
NG_008805.2:g.206159A>T , LRG_778:g.206159A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5948A>T	ENSP00000453958.2:p.Lys1983Ile
ENST00000674301.2:c.5948A>T	ENSP00000501333.2:p.Lys1983Ile
ENST00000684448.1:n.4622A>T
ENST00000316623.10:c.5948A>T MANE Select	ENSP00000325527.5:p.Lys1983Ile
ENST00000674301.1:c.947A>T	ENSP00000501333.1:p.Lys316Ile
ENST00000316623.9:c.5948A>T	ENSP00000325527.5:p.Lys1983Ile
ENST00000537463.6:c.*1711A>T	ENSP00000440294.2:n.*1711A>T
ENST00000559133.5:c.1255A>T
ENST00000560820.1:n.68A>T
NM_000138.4:c.5948A>T , LRG_778t1:c.5948A>T	NP_000129.3:p.Lys1983Ile
NM_000138.5:c.5948A>T MANE Select	NP_000129.3:p.Lys1983Ile