Canonical Allele Identifier: CA2838620333

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948874_44948875insATTTCTCCAGGGGCAGG , CM000681.2:g.44948874_44948875insATTTCTCCAGGGGCAGG	GRCh38
NC_000019.9:g.45452131_45452132insATTTCTCCAGGGGCAGG , CM000681.1:g.45452131_45452132insATTTCTCCAGGGGCAGG	GRCh37
NC_000019.8:g.50143971_50143972insATTTCTCCAGGGGCAGG	NCBI36
NG_008837.1:g.7889_7890insATTTCTCCAGGGGCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+14_215+15insATTTCTCCAGGGGCAGG (APOC2) MANE Select	ENSP00000252490.5:n.215+14_215+15insATTTCTCCAGGGGCAGG
ENST00000252490.5:c.215+14_215+15insATTTCTCCAGGGGCAGG (APOC4-APOC2)	ENSP00000252490.4:n.215+14_215+15insATTTCTCCAGGGGCAGG
ENST00000585685.5:c.*998+14_*998+15insATTTCTCCAGGGGCAGG (APOC4-APOC2)	ENSP00000467185.1:n.*998+14_*998+15insATTTCTCCAGGGGCAGG
ENST00000585786.1:c.*10_*11insATTTCTCCAGGGGCAGG (APOC2)	ENSP00000465001.1:n.*10_*11insATTTCTCCAGGGGCAGG
ENST00000589057.5:c.446+14_446+15insATTTCTCCAGGGGCAGG (APOC4-APOC2)	ENSP00000468139.1:n.446+14_446+15insATTTCTCCAGGGGCAGG
ENST00000590360.2:c.215+14_215+15insATTTCTCCAGGGGCAGG (APOC2)	ENSP00000466775.1:n.215+14_215+15insATTTCTCCAGGGGCAGG
ENST00000591597.5:c.173+56_173+57insATTTCTCCAGGGGCAGG (APOC2)	ENSP00000476835.1:n.173+56_173+57insATTTCTCCAGGGGCAGG
ENST00000592257.5:c.*9+14_*9+15insATTTCTCCAGGGGCAGG (APOC2)	ENSP00000477261.1:n.*9+14_*9+15insATTTCTCCAGGGGCAGG
NM_000483.4:c.215+14_215+15insATTTCTCCAGGGGCAGG (APOC2)	NP_000474.2:n.215+14_215+15insATTTCTCCAGGGGCAGG
NR_037932.1:n.1422+14_1422+15insATTTCTCCAGGGGCAGG (APOC4-APOC2)
NM_000483.5:c.215+14_215+15insATTTCTCCAGGGGCAGG (APOC2) MANE Select	NP_000474.2:n.215+14_215+15insATTTCTCCAGGGGCAGG