Canonical Allele Identifier: CA996271460
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

gnomAD v3: 19-44949012-C-CCT
gnomAD v4: 19-44949012-C-CCT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949013_44949014insTC , CM000681.2:g.44949013_44949014insTC GRCh38
NC_000019.9:g.45452270_45452271insTC , CM000681.1:g.45452270_45452271insTC GRCh37
NC_000019.8:g.50144110_50144111insTC NCBI36
NG_008837.1:g.8028_8029insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-146_216-145insTC (APOC2) MANE Select ENSP00000252490.5:n.216-146_216-145insTC
ENST00000252490.5:c.216-146_216-145insTC (APOC4-APOC2) ENSP00000252490.4:n.216-146_216-145insTC
ENST00000585685.5:c.*999-146_*999-145insTC (APOC4-APOC2) ENSP00000467185.1:n.*999-146_*999-145insT...
ENST00000585786.1:c.*149_*150insTC (APOC2) ENSP00000465001.1:n.*149_*150insTC
ENST00000589057.5:c.447-146_447-145insTC (APOC4-APOC2) ENSP00000468139.1:n.447-146_447-145insTC
ENST00000590360.2:c.216-146_216-145insTC (APOC2) ENSP00000466775.1:n.216-146_216-145insTC
ENST00000591597.5:c.174-146_174-145insTC (APOC2) ENSP00000476835.1:n.174-146_174-145insTC
ENST00000592257.5:c.*10-146_*10-145insTC (APOC2) ENSP00000477261.1:n.*10-146_*10-145insTC
NM_000483.4:c.216-146_216-145insTC (APOC2) NP_000474.2:n.216-146_216-145insTC
NR_037932.1:n.1423-146_1423-145insTC (APOC4-APOC2)
NM_000483.5:c.216-146_216-145insTC (APOC2) MANE Select NP_000474.2:n.216-146_216-145insTC
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