Canonical Allele Identifier: CA2585724473

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44948363-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948368_44948369dup , CM000681.2:g.44948368_44948369dup	GRCh38
NC_000019.9:g.45451625_45451626dup , CM000681.1:g.45451625_45451626dup	GRCh37
NC_000019.8:g.50143465_50143466dup	NCBI36
NG_008837.1:g.7383_7384dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-98_-13-97dup (APOC2) MANE Select	ENSP00000252490.5:n.-13-98_-13-97dup
ENST00000252490.5:c.-13-98_-13-97dup (APOC4-APOC2)	ENSP00000252490.4:n.-13-98_-13-97dup
ENST00000585685.5:c.*771-98_*771-97dup (APOC4-APOC2)	ENSP00000467185.1:n.*771-98_*771-97dup
ENST00000585786.1:c.-111_-110dup (APOC2)	ENSP00000465001.1:n.-111_-110dup
ENST00000589057.5:c.219-98_219-97dup (APOC4-APOC2)	ENSP00000468139.1:n.219-98_219-97dup
ENST00000590360.2:c.-13-98_-13-97dup (APOC2)	ENSP00000466775.1:n.-13-98_-13-97dup
ENST00000591597.5:c.-13-98_-13-97dup (APOC2)	ENSP00000476835.1:n.-13-98_-13-97dup
ENST00000592257.5:c.-13-98_-13-97dup (APOC2)	ENSP00000477261.1:n.-13-98_-13-97dup
NM_000483.4:c.-13-98_-13-97dup (APOC2)	NP_000474.2:n.-13-98_-13-97dup
NR_037932.1:n.1195-98_1195-97dup (APOC4-APOC2)
NM_000483.5:c.-13-98_-13-97dup (APOC2) MANE Select	NP_000474.2:n.-13-98_-13-97dup