Canonical Allele Identifier: CA2585724931

Gene: APOC2 APOC4-APOC2

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949010_44949011insA , CM000681.2:g.44949010_44949011insA	GRCh38
NC_000019.9:g.45452267_45452268insA , CM000681.1:g.45452267_45452268insA	GRCh37
NC_000019.8:g.50144107_50144108insA	NCBI36
NG_008837.1:g.8025_8026insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-149_216-148insA (APOC2) MANE Select	ENSP00000252490.5:n.216-149_216-148insA
ENST00000252490.5:c.216-149_216-148insA (APOC4-APOC2)	ENSP00000252490.4:n.216-149_216-148insA
ENST00000585685.5:c.*999-149_*999-148insA (APOC4-APOC2)	ENSP00000467185.1:n.*999-149_*999-148insA
ENST00000585786.1:c.*146_*147insA (APOC2)	ENSP00000465001.1:n.*146_*147insA
ENST00000589057.5:c.447-149_447-148insA (APOC4-APOC2)	ENSP00000468139.1:n.447-149_447-148insA
ENST00000590360.2:c.216-149_216-148insA (APOC2)	ENSP00000466775.1:n.216-149_216-148insA
ENST00000591597.5:c.174-149_174-148insA (APOC2)	ENSP00000476835.1:n.174-149_174-148insA
ENST00000592257.5:c.*10-149_*10-148insA (APOC2)	ENSP00000477261.1:n.*10-149_*10-148insA
NM_000483.4:c.216-149_216-148insA (APOC2)	NP_000474.2:n.216-149_216-148insA
NR_037932.1:n.1423-149_1423-148insA (APOC4-APOC2)
NM_000483.5:c.216-149_216-148insA (APOC2) MANE Select	NP_000474.2:n.216-149_216-148insA