Canonical Allele Identifier: CA2585724948

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949020-CCTCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949021_44949025del , CM000681.2:g.44949021_44949025del	GRCh38
NC_000019.9:g.45452278_45452282del , CM000681.1:g.45452278_45452282del	GRCh37
NC_000019.8:g.50144118_50144122del	NCBI36
NG_008837.1:g.8036_8040del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-138_216-134del (APOC2) MANE Select	ENSP00000252490.5:n.216-138_216-134del
ENST00000252490.5:c.216-138_216-134del (APOC4-APOC2)	ENSP00000252490.4:n.216-138_216-134del
ENST00000585685.5:c.*999-138_*999-134del (APOC4-APOC2)	ENSP00000467185.1:n.*999-138_*999-134del
ENST00000585786.1:c.*157_*161del (APOC2)	ENSP00000465001.1:n.*157_*161del
ENST00000589057.5:c.447-138_447-134del (APOC4-APOC2)	ENSP00000468139.1:n.447-138_447-134del
ENST00000590360.2:c.216-138_216-134del (APOC2)	ENSP00000466775.1:n.216-138_216-134del
ENST00000591597.5:c.174-138_174-134del (APOC2)	ENSP00000476835.1:n.174-138_174-134del
ENST00000592257.5:c.*10-138_*10-134del (APOC2)	ENSP00000477261.1:n.*10-138_*10-134del
NM_000483.4:c.216-138_216-134del (APOC2)	NP_000474.2:n.216-138_216-134del
NR_037932.1:n.1423-138_1423-134del (APOC4-APOC2)
NM_000483.5:c.216-138_216-134del (APOC2) MANE Select	NP_000474.2:n.216-138_216-134del