Canonical Allele Identifier: CA2338188857
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949114_44949115delinsGC , CM000681.2:g.44949114_44949115delinsGC GRCh38
NC_000019.9:g.45452371_45452372delinsGC , CM000681.1:g.45452371_45452372delinsGC GRCh37
NC_000019.8:g.50144211_50144212delinsGC NCBI36
NG_008837.1:g.8129_8130delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-45_216-44delinsGC (APOC2) MANE Select ENSP00000252490.5:n.216-45_216-44delinsGC...
ENST00000252490.5:c.216-45_216-44delinsGC (APOC4-APOC2) ENSP00000252490.4:n.216-45_216-44delinsGC...
ENST00000585685.5:c.*999-45_*999-44delinsGC (APOC4-APOC2) ENSP00000467185.1:n.*999-45_*999-44delins...
ENST00000585786.1:c.*250_*251delinsGC (APOC2) ENSP00000465001.1:n.*250_*251delinsGC
ENST00000589057.5:c.447-45_447-44delinsGC (APOC4-APOC2) ENSP00000468139.1:n.447-45_447-44delinsGC...
ENST00000590360.2:c.216-45_216-44delinsGC (APOC2) ENSP00000466775.1:n.216-45_216-44delinsGC...
ENST00000591597.5:c.174-45_174-44delinsGC (APOC2) ENSP00000476835.1:n.174-45_174-44delinsGC...
ENST00000592257.5:c.*10-45_*10-44delinsGC (APOC2) ENSP00000477261.1:n.*10-45_*10-44delinsGC...
NM_000483.4:c.216-45_216-44delinsGC (APOC2) NP_000474.2:n.216-45_216-44delinsGC
NR_037932.1:n.1423-45_1423-44delinsGC (APOC4-APOC2)
NM_000483.5:c.216-45_216-44delinsGC (APOC2) MANE Select NP_000474.2:n.216-45_216-44delinsGC