Canonical Allele Identifier: CA2002760271
Gene: APOC3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832768_116832769delinsTG , CM000673.2:g.116832768_116832769delinsTG GRCh38
NC_000011.9:g.116703484_116703485delinsTG , CM000673.1:g.116703484_116703485delinsTG GRCh37
NC_000011.8:g.116208694_116208695delinsTG NCBI36
NG_008949.1:g.7861_7862delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.184_185delinsTG MANE Select ENSP00000227667.2:p.Trp62=
ENST00000227667.7:c.184_185delinsTG ENSP00000227667.2:p.Trp62=
ENST00000375345.3:c.238_239delinsTG ENSP00000364494.1:p.Trp80=
ENST00000630701.1:c.238_239delinsTG ENSP00000486182.1:p.Trp80=
NM_000040.1:c.184_185delinsTG NP_000031.1:p.Trp62=
NM_000040.2:c.184_185delinsTG NP_000031.1:p.Trp62=
NM_000040.3:c.184_185delinsTG MANE Select NP_000031.1:p.Trp62=
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