Canonical Allele Identifier: CA654624861
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832955_116832956insT , CM000673.2:g.116832955_116832956insT GRCh38
NC_000011.9:g.116703671_116703672insT , CM000673.1:g.116703671_116703672insT GRCh37
NC_000011.8:g.116208881_116208882insT NCBI36
NG_008949.1:g.8048_8049insT

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*71_*72insT MANE Select ENSP00000227667.2:n.*71_*72insT
ENST00000227667.7:c.*71_*72insT ENSP00000227667.2:n.*71_*72insT
ENST00000375345.3:c.*71_*72insT ENSP00000364494.1:n.*71_*72insT
ENST00000630701.1:c.425_426insT ENSP00000486182.1:n.425_426insT
NM_000040.1:c.*71_*72insT NP_000031.1:n.*71_*72insT
NM_000040.2:c.*71_*72insT NP_000031.1:n.*71_*72insT
NM_000040.3:c.*71_*72insT MANE Select NP_000031.1:n.*71_*72insT