Canonical Allele Identifier: CA2338188681

Gene: APOC2 APOC4-APOC2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948841_44948842dup , CM000681.2:g.44948841_44948842dup	GRCh38
NC_000019.9:g.45452098_45452099dup , CM000681.1:g.45452098_45452099dup	GRCh37
NC_000019.8:g.50143938_50143939dup	NCBI36
NG_008837.1:g.7856_7857dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.196_197dup (APOC2) MANE Select	ENSP00000252490.5:p.Val67LeufsTer2
ENST00000252490.5:c.196_197dup (APOC4-APOC2)	ENSP00000252490.4:p.Val67LeufsTer2
ENST00000585685.5:c.*979_*980dup (APOC4-APOC2)	ENSP00000467185.1:n.*979_*980dup
ENST00000585786.1:c.196_197dup (APOC2)	ENSP00000465001.1:p.Val67LeufsTer2
ENST00000589057.5:c.427_428dup (APOC4-APOC2)	ENSP00000468139.1:p.Val144LeufsTer2
ENST00000590360.2:c.196_197dup (APOC2)	ENSP00000466775.1:p.Val67LeufsTer2
ENST00000591597.5:c.173+23_173+24dup (APOC2)	ENSP00000476835.1:n.173+23_173+24dup
ENST00000592257.5:c.134_135dup (APOC2)	ENSP00000477261.1:p.Cys46AlafsTer?
NM_000483.4:c.196_197dup (APOC2)	NP_000474.2:p.Val67LeufsTer2
NR_037932.1:n.1403_1404dup (APOC4-APOC2)
NM_000483.5:c.196_197dup (APOC2) MANE Select	NP_000474.2:p.Val67LeufsTer2