Canonical Allele Identifier: CA2338188751
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970353570

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948981_44948983dup , CM000681.2:g.44948981_44948983dup GRCh38
NC_000019.9:g.45452238_45452240dup , CM000681.1:g.45452238_45452240dup GRCh37
NC_000019.8:g.50144078_50144080dup NCBI36
NG_008837.1:g.7996_7998dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+121_215+123dup (APOC2) MANE Select ENSP00000252490.5:n.215+121_215+123dup
ENST00000252490.5:c.215+121_215+123dup (APOC4-APOC2) ENSP00000252490.4:n.215+121_215+123dup
ENST00000585685.5:c.*998+121_*998+123dup (APOC4-APOC2) ENSP00000467185.1:n.*998+121_*998+123dup
ENST00000585786.1:c.*117_*119dup (APOC2) ENSP00000465001.1:n.*117_*119dup
ENST00000589057.5:c.446+121_446+123dup (APOC4-APOC2) ENSP00000468139.1:n.446+121_446+123dup
ENST00000590360.2:c.215+121_215+123dup (APOC2) ENSP00000466775.1:n.215+121_215+123dup
ENST00000591597.5:c.173+163_173+165dup (APOC2) ENSP00000476835.1:n.173+163_173+165dup
ENST00000592257.5:c.*9+121_*9+123dup (APOC2) ENSP00000477261.1:n.*9+121_*9+123dup
NM_000483.4:c.215+121_215+123dup (APOC2) NP_000474.2:n.215+121_215+123dup
NR_037932.1:n.1422+121_1422+123dup (APOC4-APOC2)
NM_000483.5:c.215+121_215+123dup (APOC2) MANE Select NP_000474.2:n.215+121_215+123dup