Canonical Allele Identifier: CA2493489452
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21038320_21038341delinsTTTTTTCTTTTTTTCTTTTTTC , CM000664.2:g.21038320_21038341delinsTTTTTTCTTTTTTTCTTTTTTC GRCh38
NC_000002.11:g.21261192_21261213delinsTTTTTTCTTTTTTTCTTTTTTC , CM000664.1:g.21261192_21261213delinsTTTTTTCTTTTTTTCTTTTTTC GRCh37
NC_000002.10:g.21114697_21114718delinsTTTTTTCTTTTTTTCTTTTTTC NCBI36
NG_011793.1:g.10733_10754delinsGAAAAAAGAAAAAAAGAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-1086_384-1065delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000501110.2:n.384-1086_384-1065delinsGAAAAAAGAAAAAAAGAA...
ENST00000673882.2:c.384-1086_384-1065delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000501253.2:n.384-1086_384-1065delinsGAAAAAAGAAAAAAAGAA...
ENST00000673739.1:c.252-1086_252-1065delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000501110.1:n.252-1086_252-1065delinsGAAAAAAGAAAAAAAGAA...
ENST00000673882.1:c.252-1086_252-1065delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000501253.1:n.252-1086_252-1065delinsGAAAAAAGAAAAAAAGAA...
ENST00000233242.5:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA MANE Select ENSP00000233242.1:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAA...
ENST00000399256.4:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000382200.4:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAA...
ENST00000616098.4:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA ENSP00000477990.1:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAA...
NM_000384.2:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA NP_000375.2:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA
XM_011532809.1:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA XP_011531111.1:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA
NM_000384.3:c.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA MANE Select NP_000375.3:n.384-230_384-209delinsGAAAAAAGAAAAAAAGAAAAAA