Canonical Allele Identifier: CA633478899

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1364410523
• gnomAD v2: 19-45452503-G-GT
• gnomAD v4: 19-44949246-G-GT
• MyVariant Identifiers: chr19:g.45452503_45452504insT (hg19) ; chr19:g.44949246_44949247insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949247dup , CM000681.2:g.44949247dup	GRCh38
NC_000019.9:g.45452504dup , CM000681.1:g.45452504dup	GRCh37
NC_000019.8:g.50144344dup	NCBI36
NG_008837.1:g.8262dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.304dup (APOC2) MANE Select	ENSP00000252490.5:p.Ter102LeuextTer18
ENST00000252490.5:c.304dup (APOC4-APOC2)	ENSP00000252490.4:p.Ter102LeuextTer18
ENST00000585685.5:c.*1087dup (APOC4-APOC2)	ENSP00000467185.1:n.*1087dup
ENST00000585786.1:c.*383dup (APOC2)	ENSP00000465001.1:n.*383dup
ENST00000589057.5:c.535dup (APOC4-APOC2)	ENSP00000468139.1:p.Ter179LeuextTer18
ENST00000590360.2:c.304dup (APOC2)	ENSP00000466775.1:p.Ter102LeuextTer18
ENST00000591597.5:c.262dup (APOC2)	ENSP00000476835.1:p.Ter88LeuextTer18
ENST00000592257.5:c.*98dup (APOC2)	ENSP00000477261.1:n.*98dup
NM_000483.4:c.304dup (APOC2)	NP_000474.2:p.Ter102LeuextTer18
NR_037932.1:n.1511dup (APOC4-APOC2)
NM_000483.5:c.304dup (APOC2) MANE Select	NP_000474.2:p.Ter102LeuextTer18