Canonical Allele Identifier: CA2585725045
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949213_44949216dup , CM000681.2:g.44949213_44949216dup GRCh38
NC_000019.9:g.45452470_45452473dup , CM000681.1:g.45452470_45452473dup GRCh37
NC_000019.8:g.50144310_50144313dup NCBI36
NG_008837.1:g.8228_8231dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.270_273dup (APOC2) MANE Select ENSP00000252490.5:p.Gln92Ter
ENST00000252490.5:c.270_273dup (APOC4-APOC2) ENSP00000252490.4:p.Gln92Ter
ENST00000585685.5:c.*1053_*1056dup (APOC4-APOC2) ENSP00000467185.1:n.*1053_*1056dup
ENST00000585786.1:c.*349_*352dup (APOC2) ENSP00000465001.1:n.*349_*352dup
ENST00000589057.5:c.501_504dup (APOC4-APOC2) ENSP00000468139.1:p.Gln169Ter
ENST00000590360.2:c.270_273dup (APOC2) ENSP00000466775.1:p.Gln92Ter
ENST00000591597.5:c.228_231dup (APOC2) ENSP00000476835.1:p.Gln78Ter
ENST00000592257.5:c.*64_*67dup (APOC2) ENSP00000477261.1:n.*64_*67dup
NM_000483.4:c.270_273dup (APOC2) NP_000474.2:p.Gln92Ter
NR_037932.1:n.1477_1480dup (APOC4-APOC2)
NM_000483.5:c.270_273dup (APOC2) MANE Select NP_000474.2:p.Gln92Ter