Canonical Allele Identifier: CA2616086397
Gene: APOA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790766_116790772dup , CM000673.2:g.116790766_116790772dup GRCh38
NC_000011.9:g.116661482_116661488dup , CM000673.1:g.116661482_116661488dup GRCh37
NC_000011.8:g.116166692_116166698dup NCBI36
NG_015894.1:g.6650_6656dup
NG_015894.2:g.6650_6656dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.458_464dup MANE Select ENSP00000227665.4:p.Glu156GlyfsTer?
ENST00000433069.2:c.458_464dup ENSP00000399701.2:p.Glu156GlyfsTer?
ENST00000673688.1:c.542_548dup ENSP00000501141.1:p.Glu184GlyfsTer?
ENST00000227665.8:c.458_464dup ENSP00000227665.4:p.Glu156GlyfsTer?
ENST00000433069.1:c.458_464dup ENSP00000399701.1:p.Glu156GlyfsTer?
ENST00000542499.5:c.458_464dup ENSP00000445002.1:p.Glu156GlyfsTer?
NM_001166598.1:c.458_464dup NP_001160070.1:p.Glu156GlyfsTer?
NM_052968.4:c.458_464dup NP_443200.2:p.Glu156GlyfsTer?
NM_001166598.2:c.458_464dup NP_001160070.1:p.Glu156GlyfsTer?
NM_001371904.1:c.458_464dup MANE Select NP_001358833.1:p.Glu156GlyfsTer?
NM_052968.5:c.458_464dup NP_443200.2:p.Glu156GlyfsTer?