Canonical Allele Identifier: CA2338188271

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948024_44948026delinsACG , CM000681.2:g.44948024_44948026delinsACG	GRCh38
NC_000019.9:g.45451281_45451283delinsACG , CM000681.1:g.45451281_45451283delinsACG	GRCh37
NC_000019.8:g.50143121_50143123delinsACG	NCBI36
NG_008837.1:g.7039_7041delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-442_-13-440delinsACG (APOC2) MANE Select	ENSP00000252490.5:n.-13-442_-13-440delinsACG
ENST00000252490.5:c.-13-442_-13-440delinsACG (APOC4-APOC2)	ENSP00000252490.4:n.-13-442_-13-440delinsACG
ENST00000585685.5:c.*771-442_*771-440delinsACG (APOC4-APOC2)	ENSP00000467185.1:n.*771-442_*771-440delinsACG
ENST00000589057.5:c.219-442_219-440delinsACG (APOC4-APOC2)	ENSP00000468139.1:n.219-442_219-440delinsACG
ENST00000590360.2:c.-13-442_-13-440delinsACG (APOC2)	ENSP00000466775.1:n.-13-442_-13-440delinsACG
ENST00000591597.5:c.-13-442_-13-440delinsACG (APOC2)	ENSP00000476835.1:n.-13-442_-13-440delinsACG
ENST00000592257.5:c.-13-442_-13-440delinsACG (APOC2)	ENSP00000477261.1:n.-13-442_-13-440delinsACG
NM_000483.4:c.-13-442_-13-440delinsACG (APOC2)	NP_000474.2:n.-13-442_-13-440delinsACG
NR_037932.1:n.1195-442_1195-440delinsACG (APOC4-APOC2)
NM_000483.5:c.-13-442_-13-440delinsACG (APOC2) MANE Select	NP_000474.2:n.-13-442_-13-440delinsACG