Canonical Allele Identifier: CA2576663955

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949090_44949091insATC , CM000681.2:g.44949090_44949091insATC	GRCh38
NC_000019.9:g.45452347_45452348insATC , CM000681.1:g.45452347_45452348insATC	GRCh37
NC_000019.8:g.50144187_50144188insATC	NCBI36
NG_008837.1:g.8105_8106insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-69_216-68insATC (APOC2) MANE Select	ENSP00000252490.5:n.216-69_216-68insATC
ENST00000252490.5:c.216-69_216-68insATC (APOC4-APOC2)	ENSP00000252490.4:n.216-69_216-68insATC
ENST00000585685.5:c.*999-69_*999-68insATC (APOC4-APOC2)	ENSP00000467185.1:n.*999-69_*999-68insATC
ENST00000585786.1:c.*226_*227insATC (APOC2)	ENSP00000465001.1:n.*226_*227insATC
ENST00000589057.5:c.447-69_447-68insATC (APOC4-APOC2)	ENSP00000468139.1:n.447-69_447-68insATC
ENST00000590360.2:c.216-69_216-68insATC (APOC2)	ENSP00000466775.1:n.216-69_216-68insATC
ENST00000591597.5:c.174-69_174-68insATC (APOC2)	ENSP00000476835.1:n.174-69_174-68insATC
ENST00000592257.5:c.*10-69_*10-68insATC (APOC2)	ENSP00000477261.1:n.*10-69_*10-68insATC
NM_000483.4:c.216-69_216-68insATC (APOC2)	NP_000474.2:n.216-69_216-68insATC
NR_037932.1:n.1423-69_1423-68insATC (APOC4-APOC2)
NM_000483.5:c.216-69_216-68insATC (APOC2) MANE Select	NP_000474.2:n.216-69_216-68insATC