Canonical Allele Identifier: CA633478772

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1568634509
• gnomAD v2: 19-45451662-G-GT
• MyVariant Identifiers: chr19:g.45451662_45451663insT (hg19) ; chr19:g.44948405_44948406insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948406dup , CM000681.2:g.44948406dup	GRCh38
NC_000019.9:g.45451663dup , CM000681.1:g.45451663dup	GRCh37
NC_000019.8:g.50143503dup	NCBI36
NG_008837.1:g.7421dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.-13-60dup (APOC2) MANE Select	ENSP00000252490.5:n.-13-60dup
ENST00000252490.5:c.-13-60dup (APOC4-APOC2)	ENSP00000252490.4:n.-13-60dup
ENST00000585685.5:c.*771-60dup (APOC4-APOC2)	ENSP00000467185.1:n.*771-60dup
ENST00000585786.1:c.-73dup (APOC2)	ENSP00000465001.1:n.-73dup
ENST00000589057.5:c.219-60dup (APOC4-APOC2)	ENSP00000468139.1:n.219-60dup
ENST00000590360.2:c.-13-60dup (APOC2)	ENSP00000466775.1:n.-13-60dup
ENST00000591597.5:c.-13-60dup (APOC2)	ENSP00000476835.1:n.-13-60dup
ENST00000592257.5:c.-13-60dup (APOC2)	ENSP00000477261.1:n.-13-60dup
NM_000483.4:c.-13-60dup (APOC2)	NP_000474.2:n.-13-60dup
NR_037932.1:n.1195-60dup (APOC4-APOC2)
NM_000483.5:c.-13-60dup (APOC2) MANE Select	NP_000474.2:n.-13-60dup