Canonical Allele Identifier: CA2338188679

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948839_44948841delinsCCG , CM000681.2:g.44948839_44948841delinsCCG	GRCh38
NC_000019.9:g.45452096_45452098delinsCCG , CM000681.1:g.45452096_45452098delinsCCG	GRCh37
NC_000019.8:g.50143936_50143938delinsCCG	NCBI36
NG_008837.1:g.7854_7856delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.194_196delinsCCG (APOC2) MANE Select	ENSP00000252490.5:p.Pro65=
ENST00000252490.5:c.194_196delinsCCG (APOC4-APOC2)	ENSP00000252490.4:p.Pro65=
ENST00000585685.5:c.*977_*979delinsCCG (APOC4-APOC2)	ENSP00000467185.1:n.*977_*979delinsCCG
ENST00000585786.1:c.194_196delinsCCG (APOC2)	ENSP00000465001.1:p.Pro65=
ENST00000589057.5:c.425_427delinsCCG (APOC4-APOC2)	ENSP00000468139.1:p.Pro142=
ENST00000590360.2:c.194_196delinsCCG (APOC2)	ENSP00000466775.1:p.Pro65=
ENST00000591597.5:c.173+21_173+23delinsCCG (APOC2)	ENSP00000476835.1:n.173+21_173+23delinsCCG
ENST00000592257.5:c.132_134delinsCCG (APOC2)	ENSP00000477261.1:p.Ala44=
NM_000483.4:c.194_196delinsCCG (APOC2)	NP_000474.2:p.Pro65=
NR_037932.1:n.1401_1403delinsCCG (APOC4-APOC2)
NM_000483.5:c.194_196delinsCCG (APOC2) MANE Select	NP_000474.2:p.Pro65=