Canonical Allele Identifier: CA996270987

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948333-TGC-T
• gnomAD v4: 19-44948333-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948334_44948335del , CM000681.2:g.44948334_44948335del	GRCh38
NC_000019.9:g.45451591_45451592del , CM000681.1:g.45451591_45451592del	GRCh37
NC_000019.8:g.50143431_50143432del	NCBI36
NG_008837.1:g.7349_7350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-132_-13-131del (APOC2) MANE Select	ENSP00000252490.5:n.-13-132_-13-131del
ENST00000252490.5:c.-13-132_-13-131del (APOC4-APOC2)	ENSP00000252490.4:n.-13-132_-13-131del
ENST00000585685.5:c.*771-132_*771-131del (APOC4-APOC2)	ENSP00000467185.1:n.*771-132_*771-131del
ENST00000585786.1:c.-145_-144del (APOC2)	ENSP00000465001.1:n.-145_-144del
ENST00000589057.5:c.219-132_219-131del (APOC4-APOC2)	ENSP00000468139.1:n.219-132_219-131del
ENST00000590360.2:c.-13-132_-13-131del (APOC2)	ENSP00000466775.1:n.-13-132_-13-131del
ENST00000591597.5:c.-13-132_-13-131del (APOC2)	ENSP00000476835.1:n.-13-132_-13-131del
ENST00000592257.5:c.-13-132_-13-131del (APOC2)	ENSP00000477261.1:n.-13-132_-13-131del
NM_000483.4:c.-13-132_-13-131del (APOC2)	NP_000474.2:n.-13-132_-13-131del
NR_037932.1:n.1195-132_1195-131del (APOC4-APOC2)
NM_000483.5:c.-13-132_-13-131del (APOC2) MANE Select	NP_000474.2:n.-13-132_-13-131del