Canonical Allele Identifier: CA996270993

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948337-TGG-T
• gnomAD v4: 19-44948337-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948339_44948340del , CM000681.2:g.44948339_44948340del	GRCh38
NC_000019.9:g.45451596_45451597del , CM000681.1:g.45451596_45451597del	GRCh37
NC_000019.8:g.50143436_50143437del	NCBI36
NG_008837.1:g.7354_7355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-127_-13-126del (APOC2) MANE Select	ENSP00000252490.5:n.-13-127_-13-126del
ENST00000252490.5:c.-13-127_-13-126del (APOC4-APOC2)	ENSP00000252490.4:n.-13-127_-13-126del
ENST00000585685.5:c.*771-127_*771-126del (APOC4-APOC2)	ENSP00000467185.1:n.*771-127_*771-126del
ENST00000585786.1:c.-140_-139del (APOC2)	ENSP00000465001.1:n.-140_-139del
ENST00000589057.5:c.219-127_219-126del (APOC4-APOC2)	ENSP00000468139.1:n.219-127_219-126del
ENST00000590360.2:c.-13-127_-13-126del (APOC2)	ENSP00000466775.1:n.-13-127_-13-126del
ENST00000591597.5:c.-13-127_-13-126del (APOC2)	ENSP00000476835.1:n.-13-127_-13-126del
ENST00000592257.5:c.-13-127_-13-126del (APOC2)	ENSP00000477261.1:n.-13-127_-13-126del
NM_000483.4:c.-13-127_-13-126del (APOC2)	NP_000474.2:n.-13-127_-13-126del
NR_037932.1:n.1195-127_1195-126del (APOC4-APOC2)
NM_000483.5:c.-13-127_-13-126del (APOC2) MANE Select	NP_000474.2:n.-13-127_-13-126del