Canonical Allele Identifier: CA2814535951
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948592del , CM000681.2:g.44948592del GRCh38
NC_000019.9:g.45451849del , CM000681.1:g.45451849del GRCh37
NC_000019.8:g.50143689del NCBI36
NG_008837.1:g.7607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.55+59del (APOC2) MANE Select ENSP00000252490.5:n.55+59del
ENST00000252490.5:c.55+59del (APOC4-APOC2) ENSP00000252490.4:n.55+59del
ENST00000585685.5:c.*838+59del (APOC4-APOC2) ENSP00000467185.1:n.*838+59del
ENST00000585786.1:c.55+59del (APOC2) ENSP00000465001.1:n.55+59del
ENST00000589057.5:c.286+59del (APOC4-APOC2) ENSP00000468139.1:n.286+59del
ENST00000590360.2:c.55+59del (APOC2) ENSP00000466775.1:n.55+59del
ENST00000591597.5:c.55+59del (APOC2) ENSP00000476835.1:n.55+59del
ENST00000592257.5:c.55+59del (APOC2) ENSP00000477261.1:n.55+59del
NM_000483.4:c.55+59del (APOC2) NP_000474.2:n.55+59del
NR_037932.1:n.1262+59del (APOC4-APOC2)
NM_000483.5:c.55+59del (APOC2) MANE Select NP_000474.2:n.55+59del