Canonical Allele Identifier: CA601831224

Gene: APOA5

Linked Data

• dbSNP Id: rs1565325289
• gnomAD v2: 11-116661862-G-GCCC
• MyVariant Identifiers: chr11:g.116661862_116661863insCCC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791146_116791147insCCC , CM000673.2:g.116791146_116791147insCCC	GRCh38
NC_000011.9:g.116661862_116661863insCCC , CM000673.1:g.116661862_116661863insCCC	GRCh37
NC_000011.8:g.116167072_116167073insCCC	NCBI36
NG_015894.1:g.6274_6275insGGG
NG_015894.2:g.6274_6275insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-80_162-79insGGG MANE Select	ENSP00000227665.4:n.162-80_162-79insGGG
ENST00000433069.2:c.162-80_162-79insGGG	ENSP00000399701.2:n.162-80_162-79insGGG
ENST00000673688.1:c.166_167insGGG	ENSP00000501141.1:p.Ser56delinsTrpAla
ENST00000227665.8:c.162-80_162-79insGGG	ENSP00000227665.4:n.162-80_162-79insGGG
ENST00000433069.1:c.162-80_162-79insGGG	ENSP00000399701.1:n.162-80_162-79insGGG
ENST00000542499.5:c.162-80_162-79insGGG	ENSP00000445002.1:n.162-80_162-79insGGG
NM_001166598.1:c.162-80_162-79insGGG	NP_001160070.1:n.162-80_162-79insGGG
NM_052968.4:c.162-80_162-79insGGG	NP_443200.2:n.162-80_162-79insGGG
NM_001166598.2:c.162-80_162-79insGGG	NP_001160070.1:n.162-80_162-79insGGG
NM_001371904.1:c.162-80_162-79insGGG MANE Select	NP_001358833.1:n.162-80_162-79insGGG
NM_052968.5:c.162-80_162-79insGGG	NP_443200.2:n.162-80_162-79insGGG