Canonical Allele Identifier: CA2338188886
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949172A= , CM000681.2:g.44949172A= GRCh38
NC_000019.9:g.45452429A= , CM000681.1:g.45452429A= GRCh37
NC_000019.8:g.50144269A= NCBI36
NG_008837.1:g.8187A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.229A= (APOC2) MANE Select ENSP00000252490.5:p.Lys77=
ENST00000252490.5:c.229A= (APOC4-APOC2) ENSP00000252490.4:p.Lys77=
ENST00000585685.5:c.*1012A= (APOC4-APOC2) ENSP00000467185.1:n.*1012A=
ENST00000585786.1:c.*308A= (APOC2) ENSP00000465001.1:n.*308A=
ENST00000589057.5:c.460A= (APOC4-APOC2) ENSP00000468139.1:p.Lys154=
ENST00000590360.2:c.229A= (APOC2) ENSP00000466775.1:p.Lys77=
ENST00000591597.5:c.187A= (APOC2) ENSP00000476835.1:p.Lys63=
ENST00000592257.5:c.*23A= (APOC2) ENSP00000477261.1:n.*23A=
NM_000483.4:c.229A= (APOC2) NP_000474.2:p.Lys77=
NR_037932.1:n.1436A= (APOC4-APOC2)
NM_000483.5:c.229A= (APOC2) MANE Select NP_000474.2:p.Lys77=