Canonical Allele Identifier: CA2338188869

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949131_44949135delinsCCTCT , CM000681.2:g.44949131_44949135delinsCCTCT	GRCh38
NC_000019.9:g.45452388_45452392delinsCCTCT , CM000681.1:g.45452388_45452392delinsCCTCT	GRCh37
NC_000019.8:g.50144228_50144232delinsCCTCT	NCBI36
NG_008837.1:g.8146_8150delinsCCTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-28_216-24delinsCCTCT (APOC2) MANE Select	ENSP00000252490.5:n.216-28_216-24delinsCC...
ENST00000252490.5:c.216-28_216-24delinsCCTCT (APOC4-APOC2)	ENSP00000252490.4:n.216-28_216-24delinsCC...
ENST00000585685.5:c.*999-28_*999-24delinsCCTCT (APOC4-APOC2)	ENSP00000467185.1:n.*999-28_*999-24delins...
ENST00000585786.1:c.*267_*271delinsCCTCT (APOC2)	ENSP00000465001.1:n.*267_*271delinsCCTCT
ENST00000589057.5:c.447-28_447-24delinsCCTCT (APOC4-APOC2)	ENSP00000468139.1:n.447-28_447-24delinsCC...
ENST00000590360.2:c.216-28_216-24delinsCCTCT (APOC2)	ENSP00000466775.1:n.216-28_216-24delinsCC...
ENST00000591597.5:c.174-28_174-24delinsCCTCT (APOC2)	ENSP00000476835.1:n.174-28_174-24delinsCC...
ENST00000592257.5:c.*10-28_*10-24delinsCCTCT (APOC2)	ENSP00000477261.1:n.*10-28_*10-24delinsCC...
NM_000483.4:c.216-28_216-24delinsCCTCT (APOC2)	NP_000474.2:n.216-28_216-24delinsCCTCT
NR_037932.1:n.1423-28_1423-24delinsCCTCT (APOC4-APOC2)
NM_000483.5:c.216-28_216-24delinsCCTCT (APOC2) MANE Select	NP_000474.2:n.216-28_216-24delinsCCTCT