Canonical Allele Identifier: CA2585724814
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

gnomAD v4: 19-44948605-CCTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948609_44948611del , CM000681.2:g.44948609_44948611del GRCh38
NC_000019.9:g.45451866_45451868del , CM000681.1:g.45451866_45451868del GRCh37
NC_000019.8:g.50143706_50143708del NCBI36
NG_008837.1:g.7624_7626del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.55+76_55+78del (APOC2) MANE Select ENSP00000252490.5:n.55+76_55+78del
ENST00000252490.5:c.55+76_55+78del (APOC4-APOC2) ENSP00000252490.4:n.55+76_55+78del
ENST00000585685.5:c.*838+76_*838+78del (APOC4-APOC2) ENSP00000467185.1:n.*838+76_*838+78del
ENST00000585786.1:c.55+76_55+78del (APOC2) ENSP00000465001.1:n.55+76_55+78del
ENST00000589057.5:c.286+76_286+78del (APOC4-APOC2) ENSP00000468139.1:n.286+76_286+78del
ENST00000590360.2:c.55+76_55+78del (APOC2) ENSP00000466775.1:n.55+76_55+78del
ENST00000591597.5:c.55+76_55+78del (APOC2) ENSP00000476835.1:n.55+76_55+78del
ENST00000592257.5:c.55+76_55+78del (APOC2) ENSP00000477261.1:n.55+76_55+78del
NM_000483.4:c.55+76_55+78del (APOC2) NP_000474.2:n.55+76_55+78del
NR_037932.1:n.1262+76_1262+78del (APOC4-APOC2)
NM_000483.5:c.55+76_55+78del (APOC2) MANE Select NP_000474.2:n.55+76_55+78del
Search 100 bp 5'
Search 100 bp 3'