Canonical Allele Identifier: CA2338188529
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948384_44948385delinsTC , CM000681.2:g.44948384_44948385delinsTC GRCh38
NC_000019.9:g.45451641_45451642delinsTC , CM000681.1:g.45451641_45451642delinsTC GRCh37
NC_000019.8:g.50143481_50143482delinsTC NCBI36
NG_008837.1:g.7399_7400delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.-13-82_-13-81delinsTC (APOC2) MANE Select ENSP00000252490.5:n.-13-82_-13-81delinsTC...
ENST00000252490.5:c.-13-82_-13-81delinsTC (APOC4-APOC2) ENSP00000252490.4:n.-13-82_-13-81delinsTC...
ENST00000585685.5:c.*771-82_*771-81delinsTC (APOC4-APOC2) ENSP00000467185.1:n.*771-82_*771-81delins...
ENST00000585786.1:c.-95_-94delinsTC (APOC2) ENSP00000465001.1:n.-95_-94delinsTC
ENST00000589057.5:c.219-82_219-81delinsTC (APOC4-APOC2) ENSP00000468139.1:n.219-82_219-81delinsTC...
ENST00000590360.2:c.-13-82_-13-81delinsTC (APOC2) ENSP00000466775.1:n.-13-82_-13-81delinsTC...
ENST00000591597.5:c.-13-82_-13-81delinsTC (APOC2) ENSP00000476835.1:n.-13-82_-13-81delinsTC...
ENST00000592257.5:c.-13-82_-13-81delinsTC (APOC2) ENSP00000477261.1:n.-13-82_-13-81delinsTC...
NM_000483.4:c.-13-82_-13-81delinsTC (APOC2) NP_000474.2:n.-13-82_-13-81delinsTC
NR_037932.1:n.1195-82_1195-81delinsTC (APOC4-APOC2)
NM_000483.5:c.-13-82_-13-81delinsTC (APOC2) MANE Select NP_000474.2:n.-13-82_-13-81delinsTC