Canonical Allele Identifier: CA2175495158
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474293_48474297delinsCACAG , CM000677.2:g.48474293_48474297delinsCACAG GRCh38
NC_000015.9:g.48766490_48766494delinsCACAG , CM000677.1:g.48766490_48766494delinsCACAG GRCh37
NC_000015.8:g.46553782_46553786delinsCACAG NCBI36
NG_008805.2:g.176492_176496delinsCTGTG , LRG_778:g.176492_176496delinsCTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4168_4172delinsCTGTG ENSP00000453958.2:p.Leu1390=
ENST00000674301.2:c.4168_4172delinsCTGTG ENSP00000501333.2:p.Leu1390=
ENST00000684448.1:n.2842_2846delinsCTGTG
ENST00000316623.10:c.4168_4172delinsCTGTG MANE Select ENSP00000325527.5:p.Leu1390=
ENST00000316623.9:c.4168_4172delinsCTGTG ENSP00000325527.5:p.Leu1390=
ENST00000537463.6:c.840_844delinsCTGTG ENSP00000440294.2:p.Val280=
NM_000138.4:c.4168_4172delinsCTGTG , LRG_778t1:c.4168_4172delinsCTGTG NP_000129.3:p.Leu1390=
NM_000138.5:c.4168_4172delinsCTGTG MANE Select NP_000129.3:p.Leu1390=