Canonical Allele Identifier: CA2493489408
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21038234_21038237delinsTTTA , CM000664.2:g.21038234_21038237delinsTTTA GRCh38
NC_000002.11:g.21261106_21261109delinsTTTA , CM000664.1:g.21261106_21261109delinsTTTA GRCh37
NC_000002.10:g.21114611_21114614delinsTTTA NCBI36
NG_011793.1:g.10837_10840delinsTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-982_384-979delinsTAAA ENSP00000501110.2:n.384-982_384-979delinsTAAA
ENST00000673882.2:c.384-982_384-979delinsTAAA ENSP00000501253.2:n.384-982_384-979delinsTAAA
ENST00000673739.1:c.252-982_252-979delinsTAAA ENSP00000501110.1:n.252-982_252-979delinsTAAA
ENST00000673882.1:c.252-982_252-979delinsTAAA ENSP00000501253.1:n.252-982_252-979delinsTAAA
ENST00000233242.5:c.384-126_384-123delinsTAAA MANE Select ENSP00000233242.1:n.384-126_384-123delinsTAAA
ENST00000399256.4:c.384-126_384-123delinsTAAA ENSP00000382200.4:n.384-126_384-123delinsTAAA
ENST00000616098.4:c.384-126_384-123delinsTAAA ENSP00000477990.1:n.384-126_384-123delinsTAAA
NM_000384.2:c.384-126_384-123delinsTAAA NP_000375.2:n.384-126_384-123delinsTAAA
XM_011532809.1:c.384-126_384-123delinsTAAA XP_011531111.1:n.384-126_384-123delinsTAAA
NM_000384.3:c.384-126_384-123delinsTAAA MANE Select NP_000375.3:n.384-126_384-123delinsTAAA