Canonical Allele Identifier: CA645517010
Gene: APOB HGNC NCBI

Linked Data

COSMIC: COSM1641819
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015202_21015203insT , CM000664.2:g.21015202_21015203insT GRCh38
NC_000002.11:g.21238074_21238075insT , CM000664.1:g.21238074_21238075insT GRCh37
NC_000002.10:g.21091579_21091580insT NCBI36
NG_011793.1:g.33871_33872insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2872_*2873insA ENSP00000501110.2:n.*2872_*2873insA
ENST00000673882.2:c.*2661_*2662insA ENSP00000501253.2:n.*2661_*2662insA
ENST00000673739.1:c.3280_3281insA ENSP00000501110.1:n.3280_3281insA
ENST00000673882.1:c.3069_3070insA ENSP00000501253.1:n.3069_3070insA
ENST00000233242.5:c.3566_3567insA MANE Select ENSP00000233242.1:p.Met1189IlefsTer14
ENST00000616098.4:c.3566_3567insA ENSP00000477990.1:p.Met1189IlefsTer14
NM_000384.2:c.3566_3567insA NP_000375.2:p.Met1189IlefsTer14
XM_011532809.1:c.3566_3567insA XP_011531111.1:p.Met1189IlefsTer14
NM_000384.3:c.3566_3567insA MANE Select NP_000375.3:p.Met1189IlefsTer14
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