Canonical Allele Identifier: CA2585724469

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44948361-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948363_44948364del , CM000681.2:g.44948363_44948364del	GRCh38
NC_000019.9:g.45451620_45451621del , CM000681.1:g.45451620_45451621del	GRCh37
NC_000019.8:g.50143460_50143461del	NCBI36
NG_008837.1:g.7378_7379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-103_-13-102del (APOC2) MANE Select	ENSP00000252490.5:n.-13-103_-13-102del
ENST00000252490.5:c.-13-103_-13-102del (APOC4-APOC2)	ENSP00000252490.4:n.-13-103_-13-102del
ENST00000585685.5:c.*771-103_*771-102del (APOC4-APOC2)	ENSP00000467185.1:n.*771-103_*771-102del
ENST00000585786.1:c.-116_-115del (APOC2)	ENSP00000465001.1:n.-116_-115del
ENST00000589057.5:c.219-103_219-102del (APOC4-APOC2)	ENSP00000468139.1:n.219-103_219-102del
ENST00000590360.2:c.-13-103_-13-102del (APOC2)	ENSP00000466775.1:n.-13-103_-13-102del
ENST00000591597.5:c.-13-103_-13-102del (APOC2)	ENSP00000476835.1:n.-13-103_-13-102del
ENST00000592257.5:c.-13-103_-13-102del (APOC2)	ENSP00000477261.1:n.-13-103_-13-102del
NM_000483.4:c.-13-103_-13-102del (APOC2)	NP_000474.2:n.-13-103_-13-102del
NR_037932.1:n.1195-103_1195-102del (APOC4-APOC2)
NM_000483.5:c.-13-103_-13-102del (APOC2) MANE Select	NP_000474.2:n.-13-103_-13-102del