Canonical Allele Identifier: CA2958288061

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948487_44948488insAAA , CM000681.2:g.44948487_44948488insAAA	GRCh38
NC_000019.9:g.45451744_45451745insAAA , CM000681.1:g.45451744_45451745insAAA	GRCh37
NC_000019.8:g.50143584_50143585insAAA	NCBI36
NG_008837.1:g.7502_7503insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.9_10insAAA (APOC2) MANE Select	ENSP00000252490.5:p.Thr3_Arg4insLys
ENST00000252490.5:c.9_10insAAA (APOC4-APOC2)	ENSP00000252490.4:p.Thr3_Arg4insLys
ENST00000585685.5:c.*792_*793insAAA (APOC4-APOC2)	ENSP00000467185.1:n.*792_*793insAAA
ENST00000585786.1:c.9_10insAAA (APOC2)	ENSP00000465001.1:p.Thr3_Arg4insLys
ENST00000589057.5:c.240_241insAAA (APOC4-APOC2)	ENSP00000468139.1:p.Thr80_Arg81insLys
ENST00000590360.2:c.9_10insAAA (APOC2)	ENSP00000466775.1:p.Thr3_Arg4insLys
ENST00000591597.5:c.9_10insAAA (APOC2)	ENSP00000476835.1:p.Thr3_Arg4insLys
ENST00000592257.5:c.9_10insAAA (APOC2)	ENSP00000477261.1:p.Thr3_Arg4insLys
NM_000483.4:c.9_10insAAA (APOC2)	NP_000474.2:p.Thr3_Arg4insLys
NR_037932.1:n.1216_1217insAAA (APOC4-APOC2)
NM_000483.5:c.9_10insAAA (APOC2) MANE Select	NP_000474.2:p.Thr3_Arg4insLys