Canonical Allele Identifier: CA2338188758
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970353685

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948979_44948980insTTC , CM000681.2:g.44948979_44948980insTTC GRCh38
NC_000019.9:g.45452236_45452237insTTC , CM000681.1:g.45452236_45452237insTTC GRCh37
NC_000019.8:g.50144076_50144077insTTC NCBI36
NG_008837.1:g.7994_7995insTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+119_215+120insTTC (APOC2) MANE Select ENSP00000252490.5:n.215+119_215+120insTTC...
ENST00000252490.5:c.215+119_215+120insTTC (APOC4-APOC2) ENSP00000252490.4:n.215+119_215+120insTTC...
ENST00000585685.5:c.*998+119_*998+120insTTC (APOC4-APOC2) ENSP00000467185.1:n.*998+119_*998+120insT...
ENST00000585786.1:c.*115_*116insTTC (APOC2) ENSP00000465001.1:n.*115_*116insTTC
ENST00000589057.5:c.446+119_446+120insTTC (APOC4-APOC2) ENSP00000468139.1:n.446+119_446+120insTTC...
ENST00000590360.2:c.215+119_215+120insTTC (APOC2) ENSP00000466775.1:n.215+119_215+120insTTC...
ENST00000591597.5:c.173+161_173+162insTTC (APOC2) ENSP00000476835.1:n.173+161_173+162insTTC...
ENST00000592257.5:c.*9+119_*9+120insTTC (APOC2) ENSP00000477261.1:n.*9+119_*9+120insTTC
NM_000483.4:c.215+119_215+120insTTC (APOC2) NP_000474.2:n.215+119_215+120insTTC
NR_037932.1:n.1422+119_1422+120insTTC (APOC4-APOC2)
NM_000483.5:c.215+119_215+120insTTC (APOC2) MANE Select NP_000474.2:n.215+119_215+120insTTC