Canonical Allele Identifier: CA996271175

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970348690
• gnomAD v3: 19-44948612-A-ACCTCTGCCTCTGCCCTCTCCTCTTCTTC
• gnomAD v4: 19-44948612-A-ACCTCTGCCTCTGCCCTCTCCTCTTCTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948614_44948641dup , CM000681.2:g.44948614_44948641dup	GRCh38
NC_000019.9:g.45451871_45451898dup , CM000681.1:g.45451871_45451898dup	GRCh37
NC_000019.8:g.50143711_50143738dup	NCBI36
NG_008837.1:g.7629_7656dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.55+81_56-60dup (APOC2) MANE Select	ENSP00000252490.5:n.55+81_56-60dup
ENST00000252490.5:c.55+81_56-60dup (APOC4-APOC2)	ENSP00000252490.4:n.55+81_56-60dup
ENST00000585685.5:c.*838+81_*839-60dup (APOC4-APOC2)	ENSP00000467185.1:n.*838+81_*839-60dup
ENST00000585786.1:c.55+81_56-60dup (APOC2)	ENSP00000465001.1:n.55+81_56-60dup
ENST00000589057.5:c.286+81_287-60dup (APOC4-APOC2)	ENSP00000468139.1:n.286+81_287-60dup
ENST00000590360.2:c.55+81_56-60dup (APOC2)	ENSP00000466775.1:n.55+81_56-60dup
ENST00000591597.5:c.55+81_56-60dup (APOC2)	ENSP00000476835.1:n.55+81_56-60dup
ENST00000592257.5:c.55+81_55+108dup (APOC2)	ENSP00000477261.1:n.55+81_55+108dup
NM_000483.4:c.55+81_56-60dup (APOC2)	NP_000474.2:n.55+81_56-60dup
NR_037932.1:n.1262+81_1263-60dup (APOC4-APOC2)
NM_000483.5:c.55+81_56-60dup (APOC2) MANE Select	NP_000474.2:n.55+81_56-60dup