Canonical Allele Identifier: CA2338188771

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949004_44949078delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT , CM000681.2:g.44949004_44949078delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT	GRCh38
NC_000019.9:g.45452261_45452335delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT , CM000681.1:g.45452261_45452335delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT	GRCh37
NC_000019.8:g.50144101_50144175delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT	NCBI36
NG_008837.1:g.8019_8093delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+144_216-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2) MANE Select	ENSP00000252490.5:n.215+144_216-81delinsC...
ENST00000252490.5:c.215+144_216-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC4-APOC2)	ENSP00000252490.4:n.215+144_216-81delinsC...
ENST00000585685.5:c.*998+144_*999-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC4-APOC2)	ENSP00000467185.1:n.*998+144_*999-81delin...
ENST00000585786.1:c.*140_*214delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2)	ENSP00000465001.1:n.*140_*214delinsCCCCCA...
ENST00000589057.5:c.446+144_447-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC4-APOC2)	ENSP00000468139.1:n.446+144_447-81delinsC...
ENST00000590360.2:c.215+144_216-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2)	ENSP00000466775.1:n.215+144_216-81delinsC...
ENST00000591597.5:c.174-155_174-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2)	ENSP00000476835.1:n.174-155_174-81delinsC...
ENST00000592257.5:c.*9+144_*10-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2)	ENSP00000477261.1:n.*9+144_*10-81delinsCC...
NM_000483.4:c.215+144_216-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2)	NP_000474.2:n.215+144_216-81delinsCCCCCAG...
NR_037932.1:n.1422+144_1423-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC4-APOC2)
NM_000483.5:c.215+144_216-81delinsCCCCCAGCCCGTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT (APOC2) MANE Select	NP_000474.2:n.215+144_216-81delinsCCCCCAG...