Canonical Allele Identifier: CA2530066436

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948986_44948987insT , CM000681.2:g.44948986_44948987insT	GRCh38
NC_000019.9:g.45452243_45452244insT , CM000681.1:g.45452243_45452244insT	GRCh37
NC_000019.8:g.50144083_50144084insT	NCBI36
NG_008837.1:g.8001_8002insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+126_215+127insT (APOC2) MANE Select	ENSP00000252490.5:n.215+126_215+127insT
ENST00000252490.5:c.215+126_215+127insT (APOC4-APOC2)	ENSP00000252490.4:n.215+126_215+127insT
ENST00000585685.5:c.*998+126_*998+127insT (APOC4-APOC2)	ENSP00000467185.1:n.*998+126_*998+127insT...
ENST00000585786.1:c.*122_*123insT (APOC2)	ENSP00000465001.1:n.*122_*123insT
ENST00000589057.5:c.446+126_446+127insT (APOC4-APOC2)	ENSP00000468139.1:n.446+126_446+127insT
ENST00000590360.2:c.215+126_215+127insT (APOC2)	ENSP00000466775.1:n.215+126_215+127insT
ENST00000591597.5:c.173+168_173+169insT (APOC2)	ENSP00000476835.1:n.173+168_173+169insT
ENST00000592257.5:c.*9+126_*9+127insT (APOC2)	ENSP00000477261.1:n.*9+126_*9+127insT
NM_000483.4:c.215+126_215+127insT (APOC2)	NP_000474.2:n.215+126_215+127insT
NR_037932.1:n.1422+126_1422+127insT (APOC4-APOC2)
NM_000483.5:c.215+126_215+127insT (APOC2) MANE Select	NP_000474.2:n.215+126_215+127insT