Canonical Allele Identifier: CA308875233

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs917128904
• gnomAD v3: 19-44948384-T-TC
• gnomAD v4: 19-44948384-T-TC
• MyVariant Identifiers: chr19:g.45451641_45451642insC (hg19) ; chr19:g.44948384_44948385insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948391dup , CM000681.2:g.44948391dup	GRCh38
NC_000019.9:g.45451648dup , CM000681.1:g.45451648dup	GRCh37
NC_000019.8:g.50143488dup	NCBI36
NG_008837.1:g.7406dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.-13-75dup (APOC2) MANE Select	ENSP00000252490.5:n.-13-75dup
ENST00000252490.5:c.-13-75dup (APOC4-APOC2)	ENSP00000252490.4:n.-13-75dup
ENST00000585685.5:c.*771-75dup (APOC4-APOC2)	ENSP00000467185.1:n.*771-75dup
ENST00000585786.1:c.-88dup (APOC2)	ENSP00000465001.1:n.-88dup
ENST00000589057.5:c.219-75dup (APOC4-APOC2)	ENSP00000468139.1:n.219-75dup
ENST00000590360.2:c.-13-75dup (APOC2)	ENSP00000466775.1:n.-13-75dup
ENST00000591597.5:c.-13-75dup (APOC2)	ENSP00000476835.1:n.-13-75dup
ENST00000592257.5:c.-13-75dup (APOC2)	ENSP00000477261.1:n.-13-75dup
NM_000483.4:c.-13-75dup (APOC2)	NP_000474.2:n.-13-75dup
NR_037932.1:n.1195-75dup (APOC4-APOC2)
NM_000483.5:c.-13-75dup (APOC2) MANE Select	NP_000474.2:n.-13-75dup