Canonical Allele Identifier: CA2510603133

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949085-A-ACCCTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949098_44949134dup , CM000681.2:g.44949098_44949134dup	GRCh38
NC_000019.9:g.45452355_45452391dup , CM000681.1:g.45452355_45452391dup	GRCh37
NC_000019.8:g.50144195_50144231dup	NCBI36
NG_008837.1:g.8113_8149dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-61_216-25dup (APOC2) MANE Select	ENSP00000252490.5:n.216-61_216-25dup
ENST00000252490.5:c.216-61_216-25dup (APOC4-APOC2)	ENSP00000252490.4:n.216-61_216-25dup
ENST00000585685.5:c.*999-61_*999-25dup (APOC4-APOC2)	ENSP00000467185.1:n.*999-61_*999-25dup
ENST00000585786.1:c.*234_*270dup (APOC2)	ENSP00000465001.1:n.*234_*270dup
ENST00000589057.5:c.447-61_447-25dup (APOC4-APOC2)	ENSP00000468139.1:n.447-61_447-25dup
ENST00000590360.2:c.216-61_216-25dup (APOC2)	ENSP00000466775.1:n.216-61_216-25dup
ENST00000591597.5:c.174-61_174-25dup (APOC2)	ENSP00000476835.1:n.174-61_174-25dup
ENST00000592257.5:c.*10-61_*10-25dup (APOC2)	ENSP00000477261.1:n.*10-61_*10-25dup
NM_000483.4:c.216-61_216-25dup (APOC2)	NP_000474.2:n.216-61_216-25dup
NR_037932.1:n.1423-61_1423-25dup (APOC4-APOC2)
NM_000483.5:c.216-61_216-25dup (APOC2) MANE Select	NP_000474.2:n.216-61_216-25dup