Canonical Allele Identifier: CA392327916

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48717647T>G (hg19) ; chr15:g.48425450T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425450T>G , CM000677.2:g.48425450T>G	GRCh38
NC_000015.9:g.48717647T>G , CM000677.1:g.48717647T>G	GRCh37
NC_000015.8:g.46504939T>G	NCBI36
NG_008805.2:g.225339A>C , LRG_778:g.225339A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*180A>C	ENSP00000453958.2:n.*180A>C
ENST00000674301.2:c.*885A>C	ENSP00000501333.2:n.*885A>C
ENST00000682170.1:n.1553A>C
ENST00000682767.1:n.669A>C
ENST00000316623.10:c.7372A>C MANE Select	ENSP00000325527.5:p.Ile2458Leu
ENST00000674301.1:c.2538A>C	ENSP00000501333.1:n.2538A>C
ENST00000316623.9:c.7372A>C	ENSP00000325527.5:p.Ile2458Leu
ENST00000559133.5:c.2741A>C
NM_000138.4:c.7372A>C , LRG_778t1:c.7372A>C	NP_000129.3:p.Ile2458Leu
NM_000138.5:c.7372A>C MANE Select	NP_000129.3:p.Ile2458Leu