Canonical Allele Identifier: CA2585724870
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948923_44948925del , CM000681.2:g.44948923_44948925del GRCh38
NC_000019.9:g.45452180_45452182del , CM000681.1:g.45452180_45452182del GRCh37
NC_000019.8:g.50144020_50144022del NCBI36
NG_008837.1:g.7938_7940del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+63_215+65del (APOC2) MANE Select ENSP00000252490.5:n.215+63_215+65del
ENST00000252490.5:c.215+63_215+65del (APOC4-APOC2) ENSP00000252490.4:n.215+63_215+65del
ENST00000585685.5:c.*998+63_*998+65del (APOC4-APOC2) ENSP00000467185.1:n.*998+63_*998+65del
ENST00000585786.1:c.*59_*61del (APOC2) ENSP00000465001.1:n.*59_*61del
ENST00000589057.5:c.446+63_446+65del (APOC4-APOC2) ENSP00000468139.1:n.446+63_446+65del
ENST00000590360.2:c.215+63_215+65del (APOC2) ENSP00000466775.1:n.215+63_215+65del
ENST00000591597.5:c.173+105_173+107del (APOC2) ENSP00000476835.1:n.173+105_173+107del
ENST00000592257.5:c.*9+63_*9+65del (APOC2) ENSP00000477261.1:n.*9+63_*9+65del
NM_000483.4:c.215+63_215+65del (APOC2) NP_000474.2:n.215+63_215+65del
NR_037932.1:n.1422+63_1422+65del (APOC4-APOC2)
NM_000483.5:c.215+63_215+65del (APOC2) MANE Select NP_000474.2:n.215+63_215+65del