Canonical Allele Identifier: CA996271338
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

gnomAD v3: 19-44948950-C-CT
gnomAD v4: 19-44948950-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948950_44948951insT , CM000681.2:g.44948950_44948951insT GRCh38
NC_000019.9:g.45452207_45452208insT , CM000681.1:g.45452207_45452208insT GRCh37
NC_000019.8:g.50144047_50144048insT NCBI36
NG_008837.1:g.7965_7966insT

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+90_215+91insT (APOC2) MANE Select ENSP00000252490.5:n.215+90_215+91insT
ENST00000252490.5:c.215+90_215+91insT (APOC4-APOC2) ENSP00000252490.4:n.215+90_215+91insT
ENST00000585685.5:c.*998+90_*998+91insT (APOC4-APOC2) ENSP00000467185.1:n.*998+90_*998+91insT
ENST00000585786.1:c.*86_*87insT (APOC2) ENSP00000465001.1:n.*86_*87insT
ENST00000589057.5:c.446+90_446+91insT (APOC4-APOC2) ENSP00000468139.1:n.446+90_446+91insT
ENST00000590360.2:c.215+90_215+91insT (APOC2) ENSP00000466775.1:n.215+90_215+91insT
ENST00000591597.5:c.173+132_173+133insT (APOC2) ENSP00000476835.1:n.173+132_173+133insT
ENST00000592257.5:c.*9+90_*9+91insT (APOC2) ENSP00000477261.1:n.*9+90_*9+91insT
NM_000483.4:c.215+90_215+91insT (APOC2) NP_000474.2:n.215+90_215+91insT
NR_037932.1:n.1422+90_1422+91insT (APOC4-APOC2)
NM_000483.5:c.215+90_215+91insT (APOC2) MANE Select NP_000474.2:n.215+90_215+91insT
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