Canonical Allele Identifier: CA2585724878
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948941_44949013del , CM000681.2:g.44948941_44949013del GRCh38
NC_000019.9:g.45452198_45452270del , CM000681.1:g.45452198_45452270del GRCh37
NC_000019.8:g.50144038_50144110del NCBI36
NG_008837.1:g.7956_8028del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+81_216-146del (APOC2) MANE Select ENSP00000252490.5:n.215+81_216-146del
ENST00000252490.5:c.215+81_216-146del (APOC4-APOC2) ENSP00000252490.4:n.215+81_216-146del
ENST00000585685.5:c.*998+81_*999-146del (APOC4-APOC2) ENSP00000467185.1:n.*998+81_*999-146del
ENST00000585786.1:c.*77_*149del (APOC2) ENSP00000465001.1:n.*77_*149del
ENST00000589057.5:c.446+81_447-146del (APOC4-APOC2) ENSP00000468139.1:n.446+81_447-146del
ENST00000590360.2:c.215+81_216-146del (APOC2) ENSP00000466775.1:n.215+81_216-146del
ENST00000591597.5:c.173+123_174-146del (APOC2) ENSP00000476835.1:n.173+123_174-146del
ENST00000592257.5:c.*9+81_*10-146del (APOC2) ENSP00000477261.1:n.*9+81_*10-146del
NM_000483.4:c.215+81_216-146del (APOC2) NP_000474.2:n.215+81_216-146del
NR_037932.1:n.1422+81_1423-146del (APOC4-APOC2)
NM_000483.5:c.215+81_216-146del (APOC2) MANE Select NP_000474.2:n.215+81_216-146del