Canonical Allele Identifier: CA406294413

Gene: APOC2 APOC4-APOC2

Linked Data

• COSMIC: COSM131239
• MyVariant Identifiers: chr19:g.45452071A>G (hg19) ; chr19:g.44948814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948814A>G , CM000681.2:g.44948814A>G	GRCh38
NC_000019.9:g.45452071A>G , CM000681.1:g.45452071A>G	GRCh37
NC_000019.8:g.50143911A>G	NCBI36
NG_008837.1:g.7829A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.169A>G (APOC2) MANE Select	ENSP00000252490.5:p.Asn57Asp
ENST00000252490.5:c.169A>G (APOC4-APOC2)	ENSP00000252490.4:p.Asn57Asp
ENST00000585685.5:c.*952A>G (APOC4-APOC2)	ENSP00000467185.1:n.*952A>G
ENST00000585786.1:c.169A>G (APOC2)	ENSP00000465001.1:p.Asn57Asp
ENST00000589057.5:c.400A>G (APOC4-APOC2)	ENSP00000468139.1:p.Asn134Asp
ENST00000590360.2:c.169A>G (APOC2)	ENSP00000466775.1:p.Asn57Asp
ENST00000591597.5:c.169A>G (APOC2)	ENSP00000476835.1:p.Asn57Asp
ENST00000592257.5:c.107A>G (APOC2)	ENSP00000477261.1:p.Glu36Gly
NM_000483.4:c.169A>G (APOC2)	NP_000474.2:p.Asn57Asp
NR_037932.1:n.1376A>G (APOC4-APOC2)
NM_000483.5:c.169A>G (APOC2) MANE Select	NP_000474.2:p.Asn57Asp