Canonical Allele Identifier: CA2493472787
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002102_21002107delinsAACTTG , CM000664.2:g.21002102_21002107delinsAACTTG GRCh38
NC_000002.11:g.21224974_21224979delinsAACTTG , CM000664.1:g.21224974_21224979delinsAACTTG GRCh37
NC_000002.10:g.21078479_21078484delinsAACTTG NCBI36
NG_011793.1:g.46967_46972delinsCAAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13315_13320delinsCAAGTT MANE Select ENSP00000233242.1:p.Gln4439=
ENST00000616098.4:c.13313_13318delinsCAAGTT ENSP00000477990.1:n.13313_13318delinsCAAGTT
NM_000384.2:c.13315_13320delinsCAAGTT NP_000375.2:p.Gln4439=
XM_011532809.1:c.5870-2834_5870-2829delinsCAAGTT XP_011531111.1:n.5870-2834_5870-2829delinsCAAGTT
NM_000384.3:c.13315_13320delinsCAAGTT MANE Select NP_000375.3:p.Gln4439=
Search 100 bp 5'
Search 100 bp 3'