Canonical Allele Identifier: CA2002760362
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832955_116832956delinsGC , CM000673.2:g.116832955_116832956delinsGC GRCh38
NC_000011.9:g.116703671_116703672delinsGC , CM000673.1:g.116703671_116703672delinsGC GRCh37
NC_000011.8:g.116208881_116208882delinsGC NCBI36
NG_008949.1:g.8048_8049delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*71_*72delinsGC MANE Select ENSP00000227667.2:n.*71_*72delinsGC
ENST00000227667.7:c.*71_*72delinsGC ENSP00000227667.2:n.*71_*72delinsGC
ENST00000375345.3:c.*71_*72delinsGC ENSP00000364494.1:n.*71_*72delinsGC
ENST00000630701.1:c.425_426delinsGC ENSP00000486182.1:n.425_426delinsGC
NM_000040.1:c.*71_*72delinsGC NP_000031.1:n.*71_*72delinsGC
NM_000040.2:c.*71_*72delinsGC NP_000031.1:n.*71_*72delinsGC
NM_000040.3:c.*71_*72delinsGC MANE Select NP_000031.1:n.*71_*72delinsGC