Canonical Allele Identifier: CA2338188770

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949003_44949004delinsGC , CM000681.2:g.44949003_44949004delinsGC	GRCh38
NC_000019.9:g.45452260_45452261delinsGC , CM000681.1:g.45452260_45452261delinsGC	GRCh37
NC_000019.8:g.50144100_50144101delinsGC	NCBI36
NG_008837.1:g.8018_8019delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+143_215+144delinsGC (APOC2) MANE Select	ENSP00000252490.5:n.215+143_215+144delins...
ENST00000252490.5:c.215+143_215+144delinsGC (APOC4-APOC2)	ENSP00000252490.4:n.215+143_215+144delins...
ENST00000585685.5:c.*998+143_*998+144delinsGC (APOC4-APOC2)	ENSP00000467185.1:n.*998+143_*998+144deli...
ENST00000585786.1:c.*139_*140delinsGC (APOC2)	ENSP00000465001.1:n.*139_*140delinsGC
ENST00000589057.5:c.446+143_446+144delinsGC (APOC4-APOC2)	ENSP00000468139.1:n.446+143_446+144delins...
ENST00000590360.2:c.215+143_215+144delinsGC (APOC2)	ENSP00000466775.1:n.215+143_215+144delins...
ENST00000591597.5:c.174-156_174-155delinsGC (APOC2)	ENSP00000476835.1:n.174-156_174-155delins...
ENST00000592257.5:c.*9+143_*9+144delinsGC (APOC2)	ENSP00000477261.1:n.*9+143_*9+144delinsGC...
NM_000483.4:c.215+143_215+144delinsGC (APOC2)	NP_000474.2:n.215+143_215+144delinsGC
NR_037932.1:n.1422+143_1422+144delinsGC (APOC4-APOC2)
NM_000483.5:c.215+143_215+144delinsGC (APOC2) MANE Select	NP_000474.2:n.215+143_215+144delinsGC