Canonical Allele Identifier: CA996271346

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948953-A-ACCATCTGTGCTTTCTC
• gnomAD v4: 19-44948953-A-ACCATCTGTGCTTTCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948955_44948956insATCTGTGCTTTCTCCC , CM000681.2:g.44948955_44948956insATCTGTGCTTTCTCCC	GRCh38
NC_000019.9:g.45452212_45452213insATCTGTGCTTTCTCCC , CM000681.1:g.45452212_45452213insATCTGTGCTTTCTCCC	GRCh37
NC_000019.8:g.50144052_50144053insATCTGTGCTTTCTCCC	NCBI36
NG_008837.1:g.7970_7971insATCTGTGCTTTCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+95_215+96insATCTGTGCTTTCTCCC (APOC2) MANE Select	ENSP00000252490.5:n.215+95_215+96insATCTGTGCTTTCTCCC
ENST00000252490.5:c.215+95_215+96insATCTGTGCTTTCTCCC (APOC4-APOC2)	ENSP00000252490.4:n.215+95_215+96insATCTGTGCTTTCTCCC
ENST00000585685.5:c.*998+95_*998+96insATCTGTGCTTTCTCCC (APOC4-APOC2)	ENSP00000467185.1:n.*998+95_*998+96insATCTGTGCTTTCTCCC
ENST00000585786.1:c.*91_*92insATCTGTGCTTTCTCCC (APOC2)	ENSP00000465001.1:n.*91_*92insATCTGTGCTTTCTCCC
ENST00000589057.5:c.446+95_446+96insATCTGTGCTTTCTCCC (APOC4-APOC2)	ENSP00000468139.1:n.446+95_446+96insATCTGTGCTTTCTCCC
ENST00000590360.2:c.215+95_215+96insATCTGTGCTTTCTCCC (APOC2)	ENSP00000466775.1:n.215+95_215+96insATCTGTGCTTTCTCCC
ENST00000591597.5:c.173+137_173+138insATCTGTGCTTTCTCCC (APOC2)	ENSP00000476835.1:n.173+137_173+138insATCTGTGCTTTCTCCC
ENST00000592257.5:c.*9+95_*9+96insATCTGTGCTTTCTCCC (APOC2)	ENSP00000477261.1:n.*9+95_*9+96insATCTGTGCTTTCTCCC
NM_000483.4:c.215+95_215+96insATCTGTGCTTTCTCCC (APOC2)	NP_000474.2:n.215+95_215+96insATCTGTGCTTTCTCCC
NR_037932.1:n.1422+95_1422+96insATCTGTGCTTTCTCCC (APOC4-APOC2)
NM_000483.5:c.215+95_215+96insATCTGTGCTTTCTCCC (APOC2) MANE Select	NP_000474.2:n.215+95_215+96insATCTGTGCTTTCTCCC