Canonical Allele Identifier: CA2518327059

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949016_44949017insTTCCCCC , CM000681.2:g.44949016_44949017insTTCCCCC	GRCh38
NC_000019.9:g.45452273_45452274insTTCCCCC , CM000681.1:g.45452273_45452274insTTCCCCC	GRCh37
NC_000019.8:g.50144113_50144114insTTCCCCC	NCBI36
NG_008837.1:g.8031_8032insTTCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-143_216-142insTTCCCCC (APOC2) MANE Select	ENSP00000252490.5:n.216-143_216-142insTTCCCCC
ENST00000252490.5:c.216-143_216-142insTTCCCCC (APOC4-APOC2)	ENSP00000252490.4:n.216-143_216-142insTTCCCCC
ENST00000585685.5:c.*999-143_*999-142insTTCCCCC (APOC4-APOC2)	ENSP00000467185.1:n.*999-143_*999-142insTTCCCCC
ENST00000585786.1:c.*152_*153insTTCCCCC (APOC2)	ENSP00000465001.1:n.*152_*153insTTCCCCC
ENST00000589057.5:c.447-143_447-142insTTCCCCC (APOC4-APOC2)	ENSP00000468139.1:n.447-143_447-142insTTCCCCC
ENST00000590360.2:c.216-143_216-142insTTCCCCC (APOC2)	ENSP00000466775.1:n.216-143_216-142insTTCCCCC
ENST00000591597.5:c.174-143_174-142insTTCCCCC (APOC2)	ENSP00000476835.1:n.174-143_174-142insTTCCCCC
ENST00000592257.5:c.*10-143_*10-142insTTCCCCC (APOC2)	ENSP00000477261.1:n.*10-143_*10-142insTTCCCCC
NM_000483.4:c.216-143_216-142insTTCCCCC (APOC2)	NP_000474.2:n.216-143_216-142insTTCCCCC
NR_037932.1:n.1423-143_1423-142insTTCCCCC (APOC4-APOC2)
NM_000483.5:c.216-143_216-142insTTCCCCC (APOC2) MANE Select	NP_000474.2:n.216-143_216-142insTTCCCCC