Canonical Allele Identifier: CA2002740939
Gene: APOA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790792_116790793delinsTC , CM000673.2:g.116790792_116790793delinsTC GRCh38
NC_000011.9:g.116661508_116661509delinsTC , CM000673.1:g.116661508_116661509delinsTC GRCh37
NC_000011.8:g.116166718_116166719delinsTC NCBI36
NG_015894.1:g.6628_6629delinsGA
NG_015894.2:g.6628_6629delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.436_437delinsGA MANE Select ENSP00000227665.4:p.Glu146=
ENST00000433069.2:c.436_437delinsGA ENSP00000399701.2:p.Glu146=
ENST00000673688.1:c.520_521delinsGA ENSP00000501141.1:p.Glu174=
ENST00000227665.8:c.436_437delinsGA ENSP00000227665.4:p.Glu146=
ENST00000433069.1:c.436_437delinsGA ENSP00000399701.1:p.Glu146=
ENST00000542499.5:c.436_437delinsGA ENSP00000445002.1:p.Glu146=
NM_001166598.1:c.436_437delinsGA NP_001160070.1:p.Glu146=
NM_052968.4:c.436_437delinsGA NP_443200.2:p.Glu146=
NM_001166598.2:c.436_437delinsGA NP_001160070.1:p.Glu146=
NM_001371904.1:c.436_437delinsGA MANE Select NP_001358833.1:p.Glu146=
NM_052968.5:c.436_437delinsGA NP_443200.2:p.Glu146=