Canonical Allele Identifier: CA2958288060

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948481_44948483dup , CM000681.2:g.44948481_44948483dup	GRCh38
NC_000019.9:g.45451738_45451740dup , CM000681.1:g.45451738_45451740dup	GRCh37
NC_000019.8:g.50143578_50143580dup	NCBI36
NG_008837.1:g.7496_7498dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.3_5dup (APOC2) MANE Select	ENSP00000252490.5:p.Gly2_Thr3insGly
ENST00000252490.5:c.3_5dup (APOC4-APOC2)	ENSP00000252490.4:p.Gly2_Thr3insGly
ENST00000585685.5:c.*786_*788dup (APOC4-APOC2)	ENSP00000467185.1:n.*786_*788dup
ENST00000585786.1:c.3_5dup (APOC2)	ENSP00000465001.1:p.Gly2_Thr3insGly
ENST00000589057.5:c.234_236dup (APOC4-APOC2)	ENSP00000468139.1:p.Gly79_Thr80insGly
ENST00000590360.2:c.3_5dup (APOC2)	ENSP00000466775.1:p.Gly2_Thr3insGly
ENST00000591597.5:c.3_5dup (APOC2)	ENSP00000476835.1:p.Gly2_Thr3insGly
ENST00000592257.5:c.3_5dup (APOC2)	ENSP00000477261.1:p.Gly2_Thr3insGly
NM_000483.4:c.3_5dup (APOC2)	NP_000474.2:p.Gly2_Thr3insGly
NR_037932.1:n.1210_1212dup (APOC4-APOC2)
NM_000483.5:c.3_5dup (APOC2) MANE Select	NP_000474.2:p.Gly2_Thr3insGly