Canonical Allele Identifier: CA633478863
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1295173708

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948982_44949014del , CM000681.2:g.44948982_44949014del GRCh38
NC_000019.9:g.45452239_45452271del , CM000681.1:g.45452239_45452271del GRCh37
NC_000019.8:g.50144079_50144111del NCBI36
NG_008837.1:g.7997_8029del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+122_216-145del (APOC2) MANE Select ENSP00000252490.5:n.215+122_216-145del
ENST00000252490.5:c.215+122_216-145del (APOC4-APOC2) ENSP00000252490.4:n.215+122_216-145del
ENST00000585685.5:c.*998+122_*999-145del (APOC4-APOC2) ENSP00000467185.1:n.*998+122_*999-145del
ENST00000585786.1:c.*118_*150del (APOC2) ENSP00000465001.1:n.*118_*150del
ENST00000589057.5:c.446+122_447-145del (APOC4-APOC2) ENSP00000468139.1:n.446+122_447-145del
ENST00000590360.2:c.215+122_216-145del (APOC2) ENSP00000466775.1:n.215+122_216-145del
ENST00000591597.5:c.173+164_174-145del (APOC2) ENSP00000476835.1:n.173+164_174-145del
ENST00000592257.5:c.*9+122_*10-145del (APOC2) ENSP00000477261.1:n.*9+122_*10-145del
NM_000483.4:c.215+122_216-145del (APOC2) NP_000474.2:n.215+122_216-145del
NR_037932.1:n.1422+122_1423-145del (APOC4-APOC2)
NM_000483.5:c.215+122_216-145del (APOC2) MANE Select NP_000474.2:n.215+122_216-145del