Canonical Allele Identifier: CA2832574105
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949008dup , CM000681.2:g.44949008dup GRCh38
NC_000019.9:g.45452265dup , CM000681.1:g.45452265dup GRCh37
NC_000019.8:g.50144105dup NCBI36
NG_008837.1:g.8023dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.215+148dup (APOC2) MANE Select ENSP00000252490.5:n.215+148dup
ENST00000252490.5:c.215+148dup (APOC4-APOC2) ENSP00000252490.4:n.215+148dup
ENST00000585685.5:c.*998+148dup (APOC4-APOC2) ENSP00000467185.1:n.*998+148dup
ENST00000585786.1:c.*144dup (APOC2) ENSP00000465001.1:n.*144dup
ENST00000589057.5:c.446+148dup (APOC4-APOC2) ENSP00000468139.1:n.446+148dup
ENST00000590360.2:c.215+148dup (APOC2) ENSP00000466775.1:n.215+148dup
ENST00000591597.5:c.174-151dup (APOC2) ENSP00000476835.1:n.174-151dup
ENST00000592257.5:c.*9+148dup (APOC2) ENSP00000477261.1:n.*9+148dup
NM_000483.4:c.215+148dup (APOC2) NP_000474.2:n.215+148dup
NR_037932.1:n.1422+148dup (APOC4-APOC2)
NM_000483.5:c.215+148dup (APOC2) MANE Select NP_000474.2:n.215+148dup