Canonical Allele Identifier: CA2585724933

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949011-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949011_44949012insT , CM000681.2:g.44949011_44949012insT	GRCh38
NC_000019.9:g.45452268_45452269insT , CM000681.1:g.45452268_45452269insT	GRCh37
NC_000019.8:g.50144108_50144109insT	NCBI36
NG_008837.1:g.8026_8027insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-148_216-147insT (APOC2) MANE Select	ENSP00000252490.5:n.216-148_216-147insT
ENST00000252490.5:c.216-148_216-147insT (APOC4-APOC2)	ENSP00000252490.4:n.216-148_216-147insT
ENST00000585685.5:c.*999-148_*999-147insT (APOC4-APOC2)	ENSP00000467185.1:n.*999-148_*999-147insT
ENST00000585786.1:c.*147_*148insT (APOC2)	ENSP00000465001.1:n.*147_*148insT
ENST00000589057.5:c.447-148_447-147insT (APOC4-APOC2)	ENSP00000468139.1:n.447-148_447-147insT
ENST00000590360.2:c.216-148_216-147insT (APOC2)	ENSP00000466775.1:n.216-148_216-147insT
ENST00000591597.5:c.174-148_174-147insT (APOC2)	ENSP00000476835.1:n.174-148_174-147insT
ENST00000592257.5:c.*10-148_*10-147insT (APOC2)	ENSP00000477261.1:n.*10-148_*10-147insT
NM_000483.4:c.216-148_216-147insT (APOC2)	NP_000474.2:n.216-148_216-147insT
NR_037932.1:n.1423-148_1423-147insT (APOC4-APOC2)
NM_000483.5:c.216-148_216-147insT (APOC2) MANE Select	NP_000474.2:n.216-148_216-147insT