Canonical Allele Identifier: CA2338188942
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949278_44949280delinsGGA , CM000681.2:g.44949278_44949280delinsGGA GRCh38
NC_000019.9:g.45452535_45452537delinsGGA , CM000681.1:g.45452535_45452537delinsGGA GRCh37
NC_000019.8:g.50144375_50144377delinsGGA NCBI36
NG_008837.1:g.8293_8295delinsGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*29_*31delinsGGA (APOC2) MANE Select ENSP00000252490.5:n.*29_*31delinsGGA
ENST00000252490.5:c.*29_*31delinsGGA (APOC4-APOC2) ENSP00000252490.4:n.*29_*31delinsGGA
ENST00000585685.5:c.*1118_*1120delinsGGA (APOC4-APOC2) ENSP00000467185.1:n.*1118_*1120delinsGGA
ENST00000585786.1:c.*414_*416delinsGGA (APOC2) ENSP00000465001.1:n.*414_*416delinsGGA
ENST00000589057.5:c.*29_*31delinsGGA (APOC4-APOC2) ENSP00000468139.1:n.*29_*31delinsGGA
ENST00000590360.2:c.*29_*31delinsGGA (APOC2) ENSP00000466775.1:n.*29_*31delinsGGA
ENST00000591597.5:c.*29_*31delinsGGA (APOC2) ENSP00000476835.1:n.*29_*31delinsGGA
ENST00000592257.5:c.*129_*131delinsGGA (APOC2) ENSP00000477261.1:n.*129_*131delinsGGA
NM_000483.4:c.*29_*31delinsGGA (APOC2) NP_000474.2:n.*29_*31delinsGGA
NR_037932.1:n.1542_1544delinsGGA (APOC4-APOC2)
NM_000483.5:c.*29_*31delinsGGA (APOC2) MANE Select NP_000474.2:n.*29_*31delinsGGA