Canonical Allele Identifier: CA2338188801
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949022_44949088delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC , CM000681.2:g.44949022_44949088delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC GRCh38
NC_000019.9:g.45452279_45452345delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC , CM000681.1:g.45452279_45452345delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC GRCh37
NC_000019.8:g.50144119_50144185delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC NCBI36
NG_008837.1:g.8037_8103delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-137_216-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) MANE Select ENSP00000252490.5:n.216-137_216-71delinsT...
ENST00000252490.5:c.216-137_216-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC4-APOC2) ENSP00000252490.4:n.216-137_216-71delinsT...
ENST00000585685.5:c.*999-137_*999-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC4-APOC2) ENSP00000467185.1:n.*999-137_*999-71delin...
ENST00000585786.1:c.*158_*224delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) ENSP00000465001.1:n.*158_*224delinsTCAGAC...
ENST00000589057.5:c.447-137_447-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC4-APOC2) ENSP00000468139.1:n.447-137_447-71delinsT...
ENST00000590360.2:c.216-137_216-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) ENSP00000466775.1:n.216-137_216-71delinsT...
ENST00000591597.5:c.174-137_174-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) ENSP00000476835.1:n.174-137_174-71delinsT...
ENST00000592257.5:c.*10-137_*10-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) ENSP00000477261.1:n.*10-137_*10-71delinsT...
NM_000483.4:c.216-137_216-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) NP_000474.2:n.216-137_216-71delinsTCAGACC...
NR_037932.1:n.1423-137_1423-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC4-APOC2)
NM_000483.5:c.216-137_216-71delinsTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (APOC2) MANE Select NP_000474.2:n.216-137_216-71delinsTCAGACC...