Canonical Allele Identifier: CA996271039

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948352-G-GC
• gnomAD v4: 19-44948352-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948352_44948353insC , CM000681.2:g.44948352_44948353insC	GRCh38
NC_000019.9:g.45451609_45451610insC , CM000681.1:g.45451609_45451610insC	GRCh37
NC_000019.8:g.50143449_50143450insC	NCBI36
NG_008837.1:g.7367_7368insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-114_-13-113insC (APOC2) MANE Select	ENSP00000252490.5:n.-13-114_-13-113insC
ENST00000252490.5:c.-13-114_-13-113insC (APOC4-APOC2)	ENSP00000252490.4:n.-13-114_-13-113insC
ENST00000585685.5:c.*771-114_*771-113insC (APOC4-APOC2)	ENSP00000467185.1:n.*771-114_*771-113insC
ENST00000585786.1:c.-127_-126insC (APOC2)	ENSP00000465001.1:n.-127_-126insC
ENST00000589057.5:c.219-114_219-113insC (APOC4-APOC2)	ENSP00000468139.1:n.219-114_219-113insC
ENST00000590360.2:c.-13-114_-13-113insC (APOC2)	ENSP00000466775.1:n.-13-114_-13-113insC
ENST00000591597.5:c.-13-114_-13-113insC (APOC2)	ENSP00000476835.1:n.-13-114_-13-113insC
ENST00000592257.5:c.-13-114_-13-113insC (APOC2)	ENSP00000477261.1:n.-13-114_-13-113insC
NM_000483.4:c.-13-114_-13-113insC (APOC2)	NP_000474.2:n.-13-114_-13-113insC
NR_037932.1:n.1195-114_1195-113insC (APOC4-APOC2)
NM_000483.5:c.-13-114_-13-113insC (APOC2) MANE Select	NP_000474.2:n.-13-114_-13-113insC