Canonical Allele Identifier: CA2585724993

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949062-GACCCAGGAGTCCAGGTCCCCAGACCCTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949066_44949139del , CM000681.2:g.44949066_44949139del	GRCh38
NC_000019.9:g.45452323_45452396del , CM000681.1:g.45452323_45452396del	GRCh37
NC_000019.8:g.50144163_50144236del	NCBI36
NG_008837.1:g.8081_8154del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-93_216-20del (APOC2) MANE Select	ENSP00000252490.5:n.216-93_216-20del
ENST00000252490.5:c.216-93_216-20del (APOC4-APOC2)	ENSP00000252490.4:n.216-93_216-20del
ENST00000585685.5:c.*999-93_*999-20del (APOC4-APOC2)	ENSP00000467185.1:n.*999-93_*999-20del
ENST00000585786.1:c.*202_*275del (APOC2)	ENSP00000465001.1:n.*202_*275del
ENST00000589057.5:c.447-93_447-20del (APOC4-APOC2)	ENSP00000468139.1:n.447-93_447-20del
ENST00000590360.2:c.216-93_216-20del (APOC2)	ENSP00000466775.1:n.216-93_216-20del
ENST00000591597.5:c.174-93_174-20del (APOC2)	ENSP00000476835.1:n.174-93_174-20del
ENST00000592257.5:c.*10-93_*10-20del (APOC2)	ENSP00000477261.1:n.*10-93_*10-20del
NM_000483.4:c.216-93_216-20del (APOC2)	NP_000474.2:n.216-93_216-20del
NR_037932.1:n.1423-93_1423-20del (APOC4-APOC2)
NM_000483.5:c.216-93_216-20del (APOC2) MANE Select	NP_000474.2:n.216-93_216-20del