Canonical Allele Identifier: CA2585724928
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949009_44949010del , CM000681.2:g.44949009_44949010del GRCh38
NC_000019.9:g.45452266_45452267del , CM000681.1:g.45452266_45452267del GRCh37
NC_000019.8:g.50144106_50144107del NCBI36
NG_008837.1:g.8024_8025del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-150_216-149del (APOC2) MANE Select ENSP00000252490.5:n.216-150_216-149del
ENST00000252490.5:c.216-150_216-149del (APOC4-APOC2) ENSP00000252490.4:n.216-150_216-149del
ENST00000585685.5:c.*999-150_*999-149del (APOC4-APOC2) ENSP00000467185.1:n.*999-150_*999-149del
ENST00000585786.1:c.*145_*146del (APOC2) ENSP00000465001.1:n.*145_*146del
ENST00000589057.5:c.447-150_447-149del (APOC4-APOC2) ENSP00000468139.1:n.447-150_447-149del
ENST00000590360.2:c.216-150_216-149del (APOC2) ENSP00000466775.1:n.216-150_216-149del
ENST00000591597.5:c.174-150_174-149del (APOC2) ENSP00000476835.1:n.174-150_174-149del
ENST00000592257.5:c.*10-150_*10-149del (APOC2) ENSP00000477261.1:n.*10-150_*10-149del
NM_000483.4:c.216-150_216-149del (APOC2) NP_000474.2:n.216-150_216-149del
NR_037932.1:n.1423-150_1423-149del (APOC4-APOC2)
NM_000483.5:c.216-150_216-149del (APOC2) MANE Select NP_000474.2:n.216-150_216-149del