Canonical Allele Identifier: CA2616110947
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830741_116830755del , CM000673.2:g.116830741_116830755del GRCh38
NC_000011.9:g.116701457_116701471del , CM000673.1:g.116701457_116701471del GRCh37
NC_000011.8:g.116206667_116206681del NCBI36
NG_008949.1:g.5834_5848del

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-32_56-18del MANE Select ENSP00000227667.2:n.56-32_56-18del
ENST00000227667.7:c.56-32_56-18del ENSP00000227667.2:n.56-32_56-18del
ENST00000375345.3:c.110-32_110-18del ENSP00000364494.1:n.110-32_110-18del
ENST00000433777.5:c.56-32_56-18del ENSP00000410614.1:n.56-32_56-18del
ENST00000470144.1:n.88-32_88-18del
ENST00000630701.1:c.110-32_110-18del ENSP00000486182.1:n.110-32_110-18del
NM_000040.1:c.56-32_56-18del NP_000031.1:n.56-32_56-18del
NM_000040.2:c.56-32_56-18del NP_000031.1:n.56-32_56-18del
NM_000040.3:c.56-32_56-18del MANE Select NP_000031.1:n.56-32_56-18del