Canonical Allele Identifier: CA996271438
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948992del , CM000681.2:g.44948992del GRCh38
NC_000019.9:g.45452249del , CM000681.1:g.45452249del GRCh37
NC_000019.8:g.50144089del NCBI36
NG_008837.1:g.8007del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+132del (APOC2) MANE Select ENSP00000252490.5:n.215+132del
ENST00000252490.5:c.215+132del (APOC4-APOC2) ENSP00000252490.4:n.215+132del
ENST00000585685.5:c.*998+132del (APOC4-APOC2) ENSP00000467185.1:n.*998+132del
ENST00000585786.1:c.*128del (APOC2) ENSP00000465001.1:n.*128del
ENST00000589057.5:c.446+132del (APOC4-APOC2) ENSP00000468139.1:n.446+132del
ENST00000590360.2:c.215+132del (APOC2) ENSP00000466775.1:n.215+132del
ENST00000591597.5:c.174-167del (APOC2) ENSP00000476835.1:n.174-167del
ENST00000592257.5:c.*9+132del (APOC2) ENSP00000477261.1:n.*9+132del
NM_000483.4:c.215+132del (APOC2) NP_000474.2:n.215+132del
NR_037932.1:n.1422+132del (APOC4-APOC2)
NM_000483.5:c.215+132del (APOC2) MANE Select NP_000474.2:n.215+132del