Canonical Allele Identifier: CA2338188720
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948929_44948930delinsAG , CM000681.2:g.44948929_44948930delinsAG GRCh38
NC_000019.9:g.45452186_45452187delinsAG , CM000681.1:g.45452186_45452187delinsAG GRCh37
NC_000019.8:g.50144026_50144027delinsAG NCBI36
NG_008837.1:g.7944_7945delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+69_215+70delinsAG (APOC2) MANE Select ENSP00000252490.5:n.215+69_215+70delinsAG...
ENST00000252490.5:c.215+69_215+70delinsAG (APOC4-APOC2) ENSP00000252490.4:n.215+69_215+70delinsAG...
ENST00000585685.5:c.*998+69_*998+70delinsAG (APOC4-APOC2) ENSP00000467185.1:n.*998+69_*998+70delins...
ENST00000585786.1:c.*65_*66delinsAG (APOC2) ENSP00000465001.1:n.*65_*66delinsAG
ENST00000589057.5:c.446+69_446+70delinsAG (APOC4-APOC2) ENSP00000468139.1:n.446+69_446+70delinsAG...
ENST00000590360.2:c.215+69_215+70delinsAG (APOC2) ENSP00000466775.1:n.215+69_215+70delinsAG...
ENST00000591597.5:c.173+111_173+112delinsAG (APOC2) ENSP00000476835.1:n.173+111_173+112delins...
ENST00000592257.5:c.*9+69_*9+70delinsAG (APOC2) ENSP00000477261.1:n.*9+69_*9+70delinsAG
NM_000483.4:c.215+69_215+70delinsAG (APOC2) NP_000474.2:n.215+69_215+70delinsAG
NR_037932.1:n.1422+69_1422+70delinsAG (APOC4-APOC2)
NM_000483.5:c.215+69_215+70delinsAG (APOC2) MANE Select NP_000474.2:n.215+69_215+70delinsAG