Canonical Allele Identifier: CA2793765128
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832897_116832898insAAACACACCCAACA , CM000673.2:g.116832897_116832898insAAACACACCCAACA GRCh38
NC_000011.9:g.116703613_116703614insAAACACACCCAACA , CM000673.1:g.116703613_116703614insAAACACACCCAACA GRCh37
NC_000011.8:g.116208823_116208824insAAACACACCCAACA NCBI36
NG_008949.1:g.7990_7991insAAACACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*13_*14insAAACACACCCAACA MANE Select ENSP00000227667.2:n.*13_*14insAAACACACCCAACA
ENST00000227667.7:c.*13_*14insAAACACACCCAACA ENSP00000227667.2:n.*13_*14insAAACACACCCAACA
ENST00000375345.3:c.*13_*14insAAACACACCCAACA ENSP00000364494.1:n.*13_*14insAAACACACCCAACA
ENST00000630701.1:c.367_368insAAACACACCCAACA ENSP00000486182.1:n.367_368insAAACACACCCAACA
NM_000040.1:c.*13_*14insAAACACACCCAACA NP_000031.1:n.*13_*14insAAACACACCCAACA
NM_000040.2:c.*13_*14insAAACACACCCAACA NP_000031.1:n.*13_*14insAAACACACCCAACA
NM_000040.3:c.*13_*14insAAACACACCCAACA MANE Select NP_000031.1:n.*13_*14insAAACACACCCAACA