Canonical Allele Identifier: CA2814536014
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948903_44948904insA , CM000681.2:g.44948903_44948904insA GRCh38
NC_000019.9:g.45452160_45452161insA , CM000681.1:g.45452160_45452161insA GRCh37
NC_000019.8:g.50144000_50144001insA NCBI36
NG_008837.1:g.7918_7919insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.215+43_215+44insA (APOC2) MANE Select ENSP00000252490.5:n.215+43_215+44insA
ENST00000252490.5:c.215+43_215+44insA (APOC4-APOC2) ENSP00000252490.4:n.215+43_215+44insA
ENST00000585685.5:c.*998+43_*998+44insA (APOC4-APOC2) ENSP00000467185.1:n.*998+43_*998+44insA
ENST00000585786.1:c.*39_*40insA (APOC2) ENSP00000465001.1:n.*39_*40insA
ENST00000589057.5:c.446+43_446+44insA (APOC4-APOC2) ENSP00000468139.1:n.446+43_446+44insA
ENST00000590360.2:c.215+43_215+44insA (APOC2) ENSP00000466775.1:n.215+43_215+44insA
ENST00000591597.5:c.173+85_173+86insA (APOC2) ENSP00000476835.1:n.173+85_173+86insA
ENST00000592257.5:c.*9+43_*9+44insA (APOC2) ENSP00000477261.1:n.*9+43_*9+44insA
NM_000483.4:c.215+43_215+44insA (APOC2) NP_000474.2:n.215+43_215+44insA
NR_037932.1:n.1422+43_1422+44insA (APOC4-APOC2)
NM_000483.5:c.215+43_215+44insA (APOC2) MANE Select NP_000474.2:n.215+43_215+44insA
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