Canonical Allele Identifier: CA996271494

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v3: 19-44949018-TCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCCTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTC-T
• gnomAD v4: 19-44949018-TCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCCTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949020_44949128del , CM000681.2:g.44949020_44949128del	GRCh38
NC_000019.9:g.45452277_45452385del , CM000681.1:g.45452277_45452385del	GRCh37
NC_000019.8:g.50144117_50144225del	NCBI36
NG_008837.1:g.8035_8143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-139_216-31del (APOC2) MANE Select	ENSP00000252490.5:n.216-139_216-31del
ENST00000252490.5:c.216-139_216-31del (APOC4-APOC2)	ENSP00000252490.4:n.216-139_216-31del
ENST00000585685.5:c.*999-139_*999-31del (APOC4-APOC2)	ENSP00000467185.1:n.*999-139_*999-31del
ENST00000585786.1:c.*156_*264del (APOC2)	ENSP00000465001.1:n.*156_*264del
ENST00000589057.5:c.447-139_447-31del (APOC4-APOC2)	ENSP00000468139.1:n.447-139_447-31del
ENST00000590360.2:c.216-139_216-31del (APOC2)	ENSP00000466775.1:n.216-139_216-31del
ENST00000591597.5:c.174-139_174-31del (APOC2)	ENSP00000476835.1:n.174-139_174-31del
ENST00000592257.5:c.*10-139_*10-31del (APOC2)	ENSP00000477261.1:n.*10-139_*10-31del
NM_000483.4:c.216-139_216-31del (APOC2)	NP_000474.2:n.216-139_216-31del
NR_037932.1:n.1423-139_1423-31del (APOC4-APOC2)
NM_000483.5:c.216-139_216-31del (APOC2) MANE Select	NP_000474.2:n.216-139_216-31del