Canonical Allele Identifier: CA2585724875

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44948927-TCAGGCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948934_44948969del , CM000681.2:g.44948934_44948969del	GRCh38
NC_000019.9:g.45452191_45452226del , CM000681.1:g.45452191_45452226del	GRCh37
NC_000019.8:g.50144031_50144066del	NCBI36
NG_008837.1:g.7949_7984del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+74_215+109del (APOC2) MANE Select	ENSP00000252490.5:n.215+74_215+109del
ENST00000252490.5:c.215+74_215+109del (APOC4-APOC2)	ENSP00000252490.4:n.215+74_215+109del
ENST00000585685.5:c.*998+74_*998+109del (APOC4-APOC2)	ENSP00000467185.1:n.*998+74_*998+109del
ENST00000585786.1:c.*70_*105del (APOC2)	ENSP00000465001.1:n.*70_*105del
ENST00000589057.5:c.446+74_446+109del (APOC4-APOC2)	ENSP00000468139.1:n.446+74_446+109del
ENST00000590360.2:c.215+74_215+109del (APOC2)	ENSP00000466775.1:n.215+74_215+109del
ENST00000591597.5:c.173+116_173+151del (APOC2)	ENSP00000476835.1:n.173+116_173+151del
ENST00000592257.5:c.*9+74_*9+109del (APOC2)	ENSP00000477261.1:n.*9+74_*9+109del
NM_000483.4:c.215+74_215+109del (APOC2)	NP_000474.2:n.215+74_215+109del
NR_037932.1:n.1422+74_1422+109del (APOC4-APOC2)
NM_000483.5:c.215+74_215+109del (APOC2) MANE Select	NP_000474.2:n.215+74_215+109del