Canonical Allele Identifier: CA3039152257

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948991_44948993del , CM000681.2:g.44948991_44948993del	GRCh38
NC_000019.9:g.45452248_45452250del , CM000681.1:g.45452248_45452250del	GRCh37
NC_000019.8:g.50144088_50144090del	NCBI36
NG_008837.1:g.8006_8008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+131_215+133del (APOC2) MANE Select	ENSP00000252490.5:n.215+131_215+133del
ENST00000252490.5:c.215+131_215+133del (APOC4-APOC2)	ENSP00000252490.4:n.215+131_215+133del
ENST00000585685.5:c.*998+131_*998+133del (APOC4-APOC2)	ENSP00000467185.1:n.*998+131_*998+133del
ENST00000585786.1:c.*127_*129del (APOC2)	ENSP00000465001.1:n.*127_*129del
ENST00000589057.5:c.446+131_446+133del (APOC4-APOC2)	ENSP00000468139.1:n.446+131_446+133del
ENST00000590360.2:c.215+131_215+133del (APOC2)	ENSP00000466775.1:n.215+131_215+133del
ENST00000591597.5:c.174-168_174-166del (APOC2)	ENSP00000476835.1:n.174-168_174-166del
ENST00000592257.5:c.*9+131_*9+133del (APOC2)	ENSP00000477261.1:n.*9+131_*9+133del
NM_000483.4:c.215+131_215+133del (APOC2)	NP_000474.2:n.215+131_215+133del
NR_037932.1:n.1422+131_1422+133del (APOC4-APOC2)
NM_000483.5:c.215+131_215+133del (APOC2) MANE Select	NP_000474.2:n.215+131_215+133del