Canonical Allele Identifier: CA2338188766

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970353965

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949001_44949005dup , CM000681.2:g.44949001_44949005dup	GRCh38
NC_000019.9:g.45452258_45452262dup , CM000681.1:g.45452258_45452262dup	GRCh37
NC_000019.8:g.50144098_50144102dup	NCBI36
NG_008837.1:g.8016_8020dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+141_215+145dup (APOC2) MANE Select	ENSP00000252490.5:n.215+141_215+145dup
ENST00000252490.5:c.215+141_215+145dup (APOC4-APOC2)	ENSP00000252490.4:n.215+141_215+145dup
ENST00000585685.5:c.*998+141_*998+145dup (APOC4-APOC2)	ENSP00000467185.1:n.*998+141_*998+145dup
ENST00000585786.1:c.*137_*141dup (APOC2)	ENSP00000465001.1:n.*137_*141dup
ENST00000589057.5:c.446+141_446+145dup (APOC4-APOC2)	ENSP00000468139.1:n.446+141_446+145dup
ENST00000590360.2:c.215+141_215+145dup (APOC2)	ENSP00000466775.1:n.215+141_215+145dup
ENST00000591597.5:c.174-158_174-154dup (APOC2)	ENSP00000476835.1:n.174-158_174-154dup
ENST00000592257.5:c.*9+141_*9+145dup (APOC2)	ENSP00000477261.1:n.*9+141_*9+145dup
NM_000483.4:c.215+141_215+145dup (APOC2)	NP_000474.2:n.215+141_215+145dup
NR_037932.1:n.1422+141_1422+145dup (APOC4-APOC2)
NM_000483.5:c.215+141_215+145dup (APOC2) MANE Select	NP_000474.2:n.215+141_215+145dup