Canonical Allele Identifier: CA2585724881

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44948934-C-CCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948970_44949005dup , CM000681.2:g.44948970_44949005dup	GRCh38
NC_000019.9:g.45452227_45452262dup , CM000681.1:g.45452227_45452262dup	GRCh37
NC_000019.8:g.50144067_50144102dup	NCBI36
NG_008837.1:g.7985_8020dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+110_215+145dup (APOC2) MANE Select	ENSP00000252490.5:n.215+110_215+145dup
ENST00000252490.5:c.215+110_215+145dup (APOC4-APOC2)	ENSP00000252490.4:n.215+110_215+145dup
ENST00000585685.5:c.*998+110_*998+145dup (APOC4-APOC2)	ENSP00000467185.1:n.*998+110_*998+145dup
ENST00000585786.1:c.*106_*141dup (APOC2)	ENSP00000465001.1:n.*106_*141dup
ENST00000589057.5:c.446+110_446+145dup (APOC4-APOC2)	ENSP00000468139.1:n.446+110_446+145dup
ENST00000590360.2:c.215+110_215+145dup (APOC2)	ENSP00000466775.1:n.215+110_215+145dup
ENST00000591597.5:c.173+152_174-154dup (APOC2)	ENSP00000476835.1:n.173+152_174-154dup
ENST00000592257.5:c.*9+110_*9+145dup (APOC2)	ENSP00000477261.1:n.*9+110_*9+145dup
NM_000483.4:c.215+110_215+145dup (APOC2)	NP_000474.2:n.215+110_215+145dup
NR_037932.1:n.1422+110_1422+145dup (APOC4-APOC2)
NM_000483.5:c.215+110_215+145dup (APOC2) MANE Select	NP_000474.2:n.215+110_215+145dup