Canonical Allele Identifier: CA996271495

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1491144990
• gnomAD v3: 19-44949018-T-TCCC
• gnomAD v4: 19-44949018-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949019_44949021dup , CM000681.2:g.44949019_44949021dup	GRCh38
NC_000019.9:g.45452276_45452278dup , CM000681.1:g.45452276_45452278dup	GRCh37
NC_000019.8:g.50144116_50144118dup	NCBI36
NG_008837.1:g.8034_8036dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-140_216-138dup (APOC2) MANE Select	ENSP00000252490.5:n.216-140_216-138dup
ENST00000252490.5:c.216-140_216-138dup (APOC4-APOC2)	ENSP00000252490.4:n.216-140_216-138dup
ENST00000585685.5:c.*999-140_*999-138dup (APOC4-APOC2)	ENSP00000467185.1:n.*999-140_*999-138dup
ENST00000585786.1:c.*155_*157dup (APOC2)	ENSP00000465001.1:n.*155_*157dup
ENST00000589057.5:c.447-140_447-138dup (APOC4-APOC2)	ENSP00000468139.1:n.447-140_447-138dup
ENST00000590360.2:c.216-140_216-138dup (APOC2)	ENSP00000466775.1:n.216-140_216-138dup
ENST00000591597.5:c.174-140_174-138dup (APOC2)	ENSP00000476835.1:n.174-140_174-138dup
ENST00000592257.5:c.*10-140_*10-138dup (APOC2)	ENSP00000477261.1:n.*10-140_*10-138dup
NM_000483.4:c.216-140_216-138dup (APOC2)	NP_000474.2:n.216-140_216-138dup
NR_037932.1:n.1423-140_1423-138dup (APOC4-APOC2)
NM_000483.5:c.216-140_216-138dup (APOC2) MANE Select	NP_000474.2:n.216-140_216-138dup