Canonical Allele Identifier: CA2338188729

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970353128

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948943_44948944insTTC , CM000681.2:g.44948943_44948944insTTC	GRCh38
NC_000019.9:g.45452200_45452201insTTC , CM000681.1:g.45452200_45452201insTTC	GRCh37
NC_000019.8:g.50144040_50144041insTTC	NCBI36
NG_008837.1:g.7958_7959insTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+83_215+84insTTC (APOC2) MANE Select	ENSP00000252490.5:n.215+83_215+84insTTC
ENST00000252490.5:c.215+83_215+84insTTC (APOC4-APOC2)	ENSP00000252490.4:n.215+83_215+84insTTC
ENST00000585685.5:c.*998+83_*998+84insTTC (APOC4-APOC2)	ENSP00000467185.1:n.*998+83_*998+84insTTC...
ENST00000585786.1:c.*79_*80insTTC (APOC2)	ENSP00000465001.1:n.*79_*80insTTC
ENST00000589057.5:c.446+83_446+84insTTC (APOC4-APOC2)	ENSP00000468139.1:n.446+83_446+84insTTC
ENST00000590360.2:c.215+83_215+84insTTC (APOC2)	ENSP00000466775.1:n.215+83_215+84insTTC
ENST00000591597.5:c.173+125_173+126insTTC (APOC2)	ENSP00000476835.1:n.173+125_173+126insTTC...
ENST00000592257.5:c.*9+83_*9+84insTTC (APOC2)	ENSP00000477261.1:n.*9+83_*9+84insTTC
NM_000483.4:c.215+83_215+84insTTC (APOC2)	NP_000474.2:n.215+83_215+84insTTC
NR_037932.1:n.1422+83_1422+84insTTC (APOC4-APOC2)
NM_000483.5:c.215+83_215+84insTTC (APOC2) MANE Select	NP_000474.2:n.215+83_215+84insTTC