Canonical Allele Identifier: CA996271396

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44948975-CCCTCCTCCCT-C
• gnomAD v4: 19-44948975-CCCTCCTCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948977_44948986del , CM000681.2:g.44948977_44948986del	GRCh38
NC_000019.9:g.45452234_45452243del , CM000681.1:g.45452234_45452243del	GRCh37
NC_000019.8:g.50144074_50144083del	NCBI36
NG_008837.1:g.7992_8001del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+117_215+126del (APOC2) MANE Select	ENSP00000252490.5:n.215+117_215+126del
ENST00000252490.5:c.215+117_215+126del (APOC4-APOC2)	ENSP00000252490.4:n.215+117_215+126del
ENST00000585685.5:c.*998+117_*998+126del (APOC4-APOC2)	ENSP00000467185.1:n.*998+117_*998+126del
ENST00000585786.1:c.*113_*122del (APOC2)	ENSP00000465001.1:n.*113_*122del
ENST00000589057.5:c.446+117_446+126del (APOC4-APOC2)	ENSP00000468139.1:n.446+117_446+126del
ENST00000590360.2:c.215+117_215+126del (APOC2)	ENSP00000466775.1:n.215+117_215+126del
ENST00000591597.5:c.173+159_173+168del (APOC2)	ENSP00000476835.1:n.173+159_173+168del
ENST00000592257.5:c.*9+117_*9+126del (APOC2)	ENSP00000477261.1:n.*9+117_*9+126del
NM_000483.4:c.215+117_215+126del (APOC2)	NP_000474.2:n.215+117_215+126del
NR_037932.1:n.1422+117_1422+126del (APOC4-APOC2)
NM_000483.5:c.215+117_215+126del (APOC2) MANE Select	NP_000474.2:n.215+117_215+126del