Canonical Allele Identifier: CA882679814

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1172894559
• gnomAD v3: 19-44948628-TCTC-T
• gnomAD v4: 19-44948628-TCTC-T
• MyVariant Identifiers: chr19:g.45451886_45451888del (hg19) ; chr19:g.44948629_44948631del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948632_44948634del , CM000681.2:g.44948632_44948634del	GRCh38
NC_000019.9:g.45451889_45451891del , CM000681.1:g.45451889_45451891del	GRCh37
NC_000019.8:g.50143729_50143731del	NCBI36
NG_008837.1:g.7647_7649del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.56-69_56-67del (APOC2) MANE Select	ENSP00000252490.5:n.56-69_56-67del
ENST00000252490.5:c.56-69_56-67del (APOC4-APOC2)	ENSP00000252490.4:n.56-69_56-67del
ENST00000585685.5:c.*839-69_*839-67del (APOC4-APOC2)	ENSP00000467185.1:n.*839-69_*839-67del
ENST00000585786.1:c.56-69_56-67del (APOC2)	ENSP00000465001.1:n.56-69_56-67del
ENST00000589057.5:c.287-69_287-67del (APOC4-APOC2)	ENSP00000468139.1:n.287-69_287-67del
ENST00000590360.2:c.56-69_56-67del (APOC2)	ENSP00000466775.1:n.56-69_56-67del
ENST00000591597.5:c.56-69_56-67del (APOC2)	ENSP00000476835.1:n.56-69_56-67del
ENST00000592257.5:c.55+99_55+101del (APOC2)	ENSP00000477261.1:n.55+99_55+101del
NM_000483.4:c.56-69_56-67del (APOC2)	NP_000474.2:n.56-69_56-67del
NR_037932.1:n.1263-69_1263-67del (APOC4-APOC2)
NM_000483.5:c.56-69_56-67del (APOC2) MANE Select	NP_000474.2:n.56-69_56-67del