Canonical Allele Identifier: CA2338188756

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948978_44948979delinsTC , CM000681.2:g.44948978_44948979delinsTC	GRCh38
NC_000019.9:g.45452235_45452236delinsTC , CM000681.1:g.45452235_45452236delinsTC	GRCh37
NC_000019.8:g.50144075_50144076delinsTC	NCBI36
NG_008837.1:g.7993_7994delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+118_215+119delinsTC (APOC2) MANE Select	ENSP00000252490.5:n.215+118_215+119delinsTC
ENST00000252490.5:c.215+118_215+119delinsTC (APOC4-APOC2)	ENSP00000252490.4:n.215+118_215+119delinsTC
ENST00000585685.5:c.*998+118_*998+119delinsTC (APOC4-APOC2)	ENSP00000467185.1:n.*998+118_*998+119delinsTC
ENST00000585786.1:c.*114_*115delinsTC (APOC2)	ENSP00000465001.1:n.*114_*115delinsTC
ENST00000589057.5:c.446+118_446+119delinsTC (APOC4-APOC2)	ENSP00000468139.1:n.446+118_446+119delinsTC
ENST00000590360.2:c.215+118_215+119delinsTC (APOC2)	ENSP00000466775.1:n.215+118_215+119delinsTC
ENST00000591597.5:c.173+160_173+161delinsTC (APOC2)	ENSP00000476835.1:n.173+160_173+161delinsTC
ENST00000592257.5:c.*9+118_*9+119delinsTC (APOC2)	ENSP00000477261.1:n.*9+118_*9+119delinsTC
NM_000483.4:c.215+118_215+119delinsTC (APOC2)	NP_000474.2:n.215+118_215+119delinsTC
NR_037932.1:n.1422+118_1422+119delinsTC (APOC4-APOC2)
NM_000483.5:c.215+118_215+119delinsTC (APOC2) MANE Select	NP_000474.2:n.215+118_215+119delinsTC