Canonical Allele Identifier: CA996270988

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948335-C-CTTTTTTA
• gnomAD v4: 19-44948335-C-CTTTTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948335_44948336insTTTTTTA , CM000681.2:g.44948335_44948336insTTTTTTA	GRCh38
NC_000019.9:g.45451592_45451593insTTTTTTA , CM000681.1:g.45451592_45451593insTTTTTTA	GRCh37
NC_000019.8:g.50143432_50143433insTTTTTTA	NCBI36
NG_008837.1:g.7350_7351insTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-131_-13-130insTTTTTTA (APOC2) MANE Select	ENSP00000252490.5:n.-13-131_-13-130insTTTTTTA
ENST00000252490.5:c.-13-131_-13-130insTTTTTTA (APOC4-APOC2)	ENSP00000252490.4:n.-13-131_-13-130insTTTTTTA
ENST00000585685.5:c.*771-131_*771-130insTTTTTTA (APOC4-APOC2)	ENSP00000467185.1:n.*771-131_*771-130insTTTTTTA
ENST00000585786.1:c.-144_-143insTTTTTTA (APOC2)	ENSP00000465001.1:n.-144_-143insTTTTTTA
ENST00000589057.5:c.219-131_219-130insTTTTTTA (APOC4-APOC2)	ENSP00000468139.1:n.219-131_219-130insTTTTTTA
ENST00000590360.2:c.-13-131_-13-130insTTTTTTA (APOC2)	ENSP00000466775.1:n.-13-131_-13-130insTTTTTTA
ENST00000591597.5:c.-13-131_-13-130insTTTTTTA (APOC2)	ENSP00000476835.1:n.-13-131_-13-130insTTTTTTA
ENST00000592257.5:c.-13-131_-13-130insTTTTTTA (APOC2)	ENSP00000477261.1:n.-13-131_-13-130insTTTTTTA
NM_000483.4:c.-13-131_-13-130insTTTTTTA (APOC2)	NP_000474.2:n.-13-131_-13-130insTTTTTTA
NR_037932.1:n.1195-131_1195-130insTTTTTTA (APOC4-APOC2)
NM_000483.5:c.-13-131_-13-130insTTTTTTA (APOC2) MANE Select	NP_000474.2:n.-13-131_-13-130insTTTTTTA