Canonical Allele Identifier: CA996271392

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948973-GCCC-G
• gnomAD v4: 19-44948973-GCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948975_44948977del , CM000681.2:g.44948975_44948977del	GRCh38
NC_000019.9:g.45452232_45452234del , CM000681.1:g.45452232_45452234del	GRCh37
NC_000019.8:g.50144072_50144074del	NCBI36
NG_008837.1:g.7990_7992del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+115_215+117del (APOC2) MANE Select	ENSP00000252490.5:n.215+115_215+117del
ENST00000252490.5:c.215+115_215+117del (APOC4-APOC2)	ENSP00000252490.4:n.215+115_215+117del
ENST00000585685.5:c.*998+115_*998+117del (APOC4-APOC2)	ENSP00000467185.1:n.*998+115_*998+117del
ENST00000585786.1:c.*111_*113del (APOC2)	ENSP00000465001.1:n.*111_*113del
ENST00000589057.5:c.446+115_446+117del (APOC4-APOC2)	ENSP00000468139.1:n.446+115_446+117del
ENST00000590360.2:c.215+115_215+117del (APOC2)	ENSP00000466775.1:n.215+115_215+117del
ENST00000591597.5:c.173+157_173+159del (APOC2)	ENSP00000476835.1:n.173+157_173+159del
ENST00000592257.5:c.*9+115_*9+117del (APOC2)	ENSP00000477261.1:n.*9+115_*9+117del
NM_000483.4:c.215+115_215+117del (APOC2)	NP_000474.2:n.215+115_215+117del
NR_037932.1:n.1422+115_1422+117del (APOC4-APOC2)
NM_000483.5:c.215+115_215+117del (APOC2) MANE Select	NP_000474.2:n.215+115_215+117del