Canonical Allele Identifier: CA2512444350

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948970_44948974del , CM000681.2:g.44948970_44948974del	GRCh38
NC_000019.9:g.45452227_45452231del , CM000681.1:g.45452227_45452231del	GRCh37
NC_000019.8:g.50144067_50144071del	NCBI36
NG_008837.1:g.7985_7989del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+110_215+114del (APOC2) MANE Select	ENSP00000252490.5:n.215+110_215+114del
ENST00000252490.5:c.215+110_215+114del (APOC4-APOC2)	ENSP00000252490.4:n.215+110_215+114del
ENST00000585685.5:c.*998+110_*998+114del (APOC4-APOC2)	ENSP00000467185.1:n.*998+110_*998+114del
ENST00000585786.1:c.*106_*110del (APOC2)	ENSP00000465001.1:n.*106_*110del
ENST00000589057.5:c.446+110_446+114del (APOC4-APOC2)	ENSP00000468139.1:n.446+110_446+114del
ENST00000590360.2:c.215+110_215+114del (APOC2)	ENSP00000466775.1:n.215+110_215+114del
ENST00000591597.5:c.173+152_173+156del (APOC2)	ENSP00000476835.1:n.173+152_173+156del
ENST00000592257.5:c.*9+110_*9+114del (APOC2)	ENSP00000477261.1:n.*9+110_*9+114del
NM_000483.4:c.215+110_215+114del (APOC2)	NP_000474.2:n.215+110_215+114del
NR_037932.1:n.1422+110_1422+114del (APOC4-APOC2)
NM_000483.5:c.215+110_215+114del (APOC2) MANE Select	NP_000474.2:n.215+110_215+114del