Canonical Allele Identifier: CA2493481678
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021173_21021174delinsGA , CM000664.2:g.21021173_21021174delinsGA GRCh38
NC_000002.11:g.21244045_21244046delinsGA , CM000664.1:g.21244045_21244046delinsGA GRCh37
NC_000002.10:g.21097550_21097551delinsGA NCBI36
NG_011793.1:g.27900_27901delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*2123-1269_*2123-1268delinsTC ENSP00000501110.2:n.*2123-1269_*2123-1268...
ENST00000673882.2:c.*2123-1269_*2123-1268delinsTC ENSP00000501253.2:n.*2123-1269_*2123-1268...
ENST00000673739.1:c.2531-1269_2531-1268delinsTC ENSP00000501110.1:n.2531-1269_2531-1268de...
ENST00000673882.1:c.2531-1269_2531-1268delinsTC ENSP00000501253.1:n.2531-1269_2531-1268de...
ENST00000233242.5:c.2817-1269_2817-1268delinsTC MANE Select ENSP00000233242.1:n.2817-1269_2817-1268de...
ENST00000616098.4:c.2817-1269_2817-1268delinsTC ENSP00000477990.1:n.2817-1269_2817-1268de...
NM_000384.2:c.2817-1269_2817-1268delinsTC NP_000375.2:n.2817-1269_2817-1268delinsTC...
XM_011532809.1:c.2817-1269_2817-1268delinsTC XP_011531111.1:n.2817-1269_2817-1268delin...
NM_000384.3:c.2817-1269_2817-1268delinsTC MANE Select NP_000375.3:n.2817-1269_2817-1268delinsTC...