Canonical Allele Identifier: CA2493476701
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010424_21010425delinsCT , CM000664.2:g.21010424_21010425delinsCT GRCh38
NC_000002.11:g.21233296_21233297delinsCT , CM000664.1:g.21233296_21233297delinsCT GRCh37
NC_000002.10:g.21086801_21086802delinsCT NCBI36
NG_011793.1:g.38649_38650delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6443_6444delinsAG MANE Select ENSP00000233242.1:p.Lys2148=
ENST00000616098.4:c.6443_6444delinsAG ENSP00000477990.1:p.Lys2148=
NM_000384.2:c.6443_6444delinsAG NP_000375.2:p.Lys2148=
XM_011532809.1:c.5869+308_5869+309delinsAG XP_011531111.1:n.5869+308_5869+309delinsAG
NM_000384.3:c.6443_6444delinsAG MANE Select NP_000375.3:p.Lys2148=