Canonical Allele Identifier: CA2585724976

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949041-CCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949048_44949084del , CM000681.2:g.44949048_44949084del	GRCh38
NC_000019.9:g.45452305_45452341del , CM000681.1:g.45452305_45452341del	GRCh37
NC_000019.8:g.50144145_50144181del	NCBI36
NG_008837.1:g.8063_8099del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-111_216-75del (APOC2) MANE Select	ENSP00000252490.5:n.216-111_216-75del
ENST00000252490.5:c.216-111_216-75del (APOC4-APOC2)	ENSP00000252490.4:n.216-111_216-75del
ENST00000585685.5:c.*999-111_*999-75del (APOC4-APOC2)	ENSP00000467185.1:n.*999-111_*999-75del
ENST00000585786.1:c.*184_*220del (APOC2)	ENSP00000465001.1:n.*184_*220del
ENST00000589057.5:c.447-111_447-75del (APOC4-APOC2)	ENSP00000468139.1:n.447-111_447-75del
ENST00000590360.2:c.216-111_216-75del (APOC2)	ENSP00000466775.1:n.216-111_216-75del
ENST00000591597.5:c.174-111_174-75del (APOC2)	ENSP00000476835.1:n.174-111_174-75del
ENST00000592257.5:c.*10-111_*10-75del (APOC2)	ENSP00000477261.1:n.*10-111_*10-75del
NM_000483.4:c.216-111_216-75del (APOC2)	NP_000474.2:n.216-111_216-75del
NR_037932.1:n.1423-111_1423-75del (APOC4-APOC2)
NM_000483.5:c.216-111_216-75del (APOC2) MANE Select	NP_000474.2:n.216-111_216-75del