Canonical Allele Identifier: CA996271357

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948967-G-GT
• gnomAD v4: 19-44948967-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948967_44948968insT , CM000681.2:g.44948967_44948968insT	GRCh38
NC_000019.9:g.45452224_45452225insT , CM000681.1:g.45452224_45452225insT	GRCh37
NC_000019.8:g.50144064_50144065insT	NCBI36
NG_008837.1:g.7982_7983insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+107_215+108insT (APOC2) MANE Select	ENSP00000252490.5:n.215+107_215+108insT
ENST00000252490.5:c.215+107_215+108insT (APOC4-APOC2)	ENSP00000252490.4:n.215+107_215+108insT
ENST00000585685.5:c.*998+107_*998+108insT (APOC4-APOC2)	ENSP00000467185.1:n.*998+107_*998+108insT...
ENST00000585786.1:c.*103_*104insT (APOC2)	ENSP00000465001.1:n.*103_*104insT
ENST00000589057.5:c.446+107_446+108insT (APOC4-APOC2)	ENSP00000468139.1:n.446+107_446+108insT
ENST00000590360.2:c.215+107_215+108insT (APOC2)	ENSP00000466775.1:n.215+107_215+108insT
ENST00000591597.5:c.173+149_173+150insT (APOC2)	ENSP00000476835.1:n.173+149_173+150insT
ENST00000592257.5:c.*9+107_*9+108insT (APOC2)	ENSP00000477261.1:n.*9+107_*9+108insT
NM_000483.4:c.215+107_215+108insT (APOC2)	NP_000474.2:n.215+107_215+108insT
NR_037932.1:n.1422+107_1422+108insT (APOC4-APOC2)
NM_000483.5:c.215+107_215+108insT (APOC2) MANE Select	NP_000474.2:n.215+107_215+108insT