Canonical Allele Identifier: CA633478852
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1458554090

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948970_44949005del , CM000681.2:g.44948970_44949005del GRCh38
NC_000019.9:g.45452227_45452262del , CM000681.1:g.45452227_45452262del GRCh37
NC_000019.8:g.50144067_50144102del NCBI36
NG_008837.1:g.7985_8020del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+110_215+145del (APOC2) MANE Select ENSP00000252490.5:n.215+110_215+145del
ENST00000252490.5:c.215+110_215+145del (APOC4-APOC2) ENSP00000252490.4:n.215+110_215+145del
ENST00000585685.5:c.*998+110_*998+145del (APOC4-APOC2) ENSP00000467185.1:n.*998+110_*998+145del
ENST00000585786.1:c.*106_*141del (APOC2) ENSP00000465001.1:n.*106_*141del
ENST00000589057.5:c.446+110_446+145del (APOC4-APOC2) ENSP00000468139.1:n.446+110_446+145del
ENST00000590360.2:c.215+110_215+145del (APOC2) ENSP00000466775.1:n.215+110_215+145del
ENST00000591597.5:c.173+152_174-154del (APOC2) ENSP00000476835.1:n.173+152_174-154del
ENST00000592257.5:c.*9+110_*9+145del (APOC2) ENSP00000477261.1:n.*9+110_*9+145del
NM_000483.4:c.215+110_215+145del (APOC2) NP_000474.2:n.215+110_215+145del
NR_037932.1:n.1422+110_1422+145del (APOC4-APOC2)
NM_000483.5:c.215+110_215+145del (APOC2) MANE Select NP_000474.2:n.215+110_215+145del