Canonical Allele Identifier: CA996271022

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948344-CTTGACT-C
• gnomAD v4: 19-44948344-CTTGACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948345_44948350del , CM000681.2:g.44948345_44948350del	GRCh38
NC_000019.9:g.45451602_45451607del , CM000681.1:g.45451602_45451607del	GRCh37
NC_000019.8:g.50143442_50143447del	NCBI36
NG_008837.1:g.7360_7365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-121_-13-116del (APOC2) MANE Select	ENSP00000252490.5:n.-13-121_-13-116del
ENST00000252490.5:c.-13-121_-13-116del (APOC4-APOC2)	ENSP00000252490.4:n.-13-121_-13-116del
ENST00000585685.5:c.*771-121_*771-116del (APOC4-APOC2)	ENSP00000467185.1:n.*771-121_*771-116del
ENST00000585786.1:c.-134_-129del (APOC2)	ENSP00000465001.1:n.-134_-129del
ENST00000589057.5:c.219-121_219-116del (APOC4-APOC2)	ENSP00000468139.1:n.219-121_219-116del
ENST00000590360.2:c.-13-121_-13-116del (APOC2)	ENSP00000466775.1:n.-13-121_-13-116del
ENST00000591597.5:c.-13-121_-13-116del (APOC2)	ENSP00000476835.1:n.-13-121_-13-116del
ENST00000592257.5:c.-13-121_-13-116del (APOC2)	ENSP00000477261.1:n.-13-121_-13-116del
NM_000483.4:c.-13-121_-13-116del (APOC2)	NP_000474.2:n.-13-121_-13-116del
NR_037932.1:n.1195-121_1195-116del (APOC4-APOC2)
NM_000483.5:c.-13-121_-13-116del (APOC2) MANE Select	NP_000474.2:n.-13-121_-13-116del