Canonical Allele Identifier: CA3039152258

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949006_44949009del , CM000681.2:g.44949006_44949009del	GRCh38
NC_000019.9:g.45452263_45452266del , CM000681.1:g.45452263_45452266del	GRCh37
NC_000019.8:g.50144103_50144106del	NCBI36
NG_008837.1:g.8021_8024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+146_216-150del (APOC2) MANE Select	ENSP00000252490.5:n.215+146_216-150del
ENST00000252490.5:c.215+146_216-150del (APOC4-APOC2)	ENSP00000252490.4:n.215+146_216-150del
ENST00000585685.5:c.*998+146_*999-150del (APOC4-APOC2)	ENSP00000467185.1:n.*998+146_*999-150del
ENST00000585786.1:c.*142_*145del (APOC2)	ENSP00000465001.1:n.*142_*145del
ENST00000589057.5:c.446+146_447-150del (APOC4-APOC2)	ENSP00000468139.1:n.446+146_447-150del
ENST00000590360.2:c.215+146_216-150del (APOC2)	ENSP00000466775.1:n.215+146_216-150del
ENST00000591597.5:c.174-153_174-150del (APOC2)	ENSP00000476835.1:n.174-153_174-150del
ENST00000592257.5:c.*9+146_*10-150del (APOC2)	ENSP00000477261.1:n.*9+146_*10-150del
NM_000483.4:c.215+146_216-150del (APOC2)	NP_000474.2:n.215+146_216-150del
NR_037932.1:n.1422+146_1423-150del (APOC4-APOC2)
NM_000483.5:c.215+146_216-150del (APOC2) MANE Select	NP_000474.2:n.215+146_216-150del