Canonical Allele Identifier: CA2585724796

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44948549-CGGGGAGGGAAGCCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948558_44948572del , CM000681.2:g.44948558_44948572del	GRCh38
NC_000019.9:g.45451815_45451829del , CM000681.1:g.45451815_45451829del	GRCh37
NC_000019.8:g.50143655_50143669del	NCBI36
NG_008837.1:g.7573_7587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.55+25_55+39del (APOC2) MANE Select	ENSP00000252490.5:n.55+25_55+39del
ENST00000252490.5:c.55+25_55+39del (APOC4-APOC2)	ENSP00000252490.4:n.55+25_55+39del
ENST00000585685.5:c.*838+25_*838+39del (APOC4-APOC2)	ENSP00000467185.1:n.*838+25_*838+39del
ENST00000585786.1:c.55+25_55+39del (APOC2)	ENSP00000465001.1:n.55+25_55+39del
ENST00000589057.5:c.286+25_286+39del (APOC4-APOC2)	ENSP00000468139.1:n.286+25_286+39del
ENST00000590360.2:c.55+25_55+39del (APOC2)	ENSP00000466775.1:n.55+25_55+39del
ENST00000591597.5:c.55+25_55+39del (APOC2)	ENSP00000476835.1:n.55+25_55+39del
ENST00000592257.5:c.55+25_55+39del (APOC2)	ENSP00000477261.1:n.55+25_55+39del
NM_000483.4:c.55+25_55+39del (APOC2)	NP_000474.2:n.55+25_55+39del
NR_037932.1:n.1262+25_1262+39del (APOC4-APOC2)
NM_000483.5:c.55+25_55+39del (APOC2) MANE Select	NP_000474.2:n.55+25_55+39del