Canonical Allele Identifier: CA2574986401
Gene: APOA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116791090del , CM000673.2:g.116791090del GRCh38
NC_000011.9:g.116661806del , CM000673.1:g.116661806del GRCh37
NC_000011.8:g.116167016del NCBI36
NG_015894.1:g.6331del
NG_015894.2:g.6331del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.162-23del MANE Select ENSP00000227665.4:n.162-23del
ENST00000433069.2:c.162-23del ENSP00000399701.2:n.162-23del
ENST00000673688.1:c.223del ENSP00000501141.1:p.Trp75GlyfsTer10
ENST00000227665.8:c.162-23del ENSP00000227665.4:n.162-23del
ENST00000433069.1:c.162-23del ENSP00000399701.1:n.162-23del
ENST00000542499.5:c.162-23del ENSP00000445002.1:n.162-23del
NM_001166598.1:c.162-23del NP_001160070.1:n.162-23del
NM_052968.4:c.162-23del NP_443200.2:n.162-23del
NM_001166598.2:c.162-23del NP_001160070.1:n.162-23del
NM_001371904.1:c.162-23del MANE Select NP_001358833.1:n.162-23del
NM_052968.5:c.162-23del NP_443200.2:n.162-23del