Canonical Allele Identifier: CA3039152254

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948961_44948962insAAA , CM000681.2:g.44948961_44948962insAAA	GRCh38
NC_000019.9:g.45452218_45452219insAAA , CM000681.1:g.45452218_45452219insAAA	GRCh37
NC_000019.8:g.50144058_50144059insAAA	NCBI36
NG_008837.1:g.7976_7977insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+101_215+102insAAA (APOC2) MANE Select	ENSP00000252490.5:n.215+101_215+102insAAA
ENST00000252490.5:c.215+101_215+102insAAA (APOC4-APOC2)	ENSP00000252490.4:n.215+101_215+102insAAA
ENST00000585685.5:c.*998+101_*998+102insAAA (APOC4-APOC2)	ENSP00000467185.1:n.*998+101_*998+102insAAA
ENST00000585786.1:c.*97_*98insAAA (APOC2)	ENSP00000465001.1:n.*97_*98insAAA
ENST00000589057.5:c.446+101_446+102insAAA (APOC4-APOC2)	ENSP00000468139.1:n.446+101_446+102insAAA
ENST00000590360.2:c.215+101_215+102insAAA (APOC2)	ENSP00000466775.1:n.215+101_215+102insAAA
ENST00000591597.5:c.173+143_173+144insAAA (APOC2)	ENSP00000476835.1:n.173+143_173+144insAAA
ENST00000592257.5:c.*9+101_*9+102insAAA (APOC2)	ENSP00000477261.1:n.*9+101_*9+102insAAA
NM_000483.4:c.215+101_215+102insAAA (APOC2)	NP_000474.2:n.215+101_215+102insAAA
NR_037932.1:n.1422+101_1422+102insAAA (APOC4-APOC2)
NM_000483.5:c.215+101_215+102insAAA (APOC2) MANE Select	NP_000474.2:n.215+101_215+102insAAA