Canonical Allele Identifier: CA2493476946
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010999_21011003delinsTAGAC , CM000664.2:g.21010999_21011003delinsTAGAC GRCh38
NC_000002.11:g.21233871_21233875delinsTAGAC , CM000664.1:g.21233871_21233875delinsTAGAC GRCh37
NC_000002.10:g.21087376_21087380delinsTAGAC NCBI36
NG_011793.1:g.38071_38075delinsGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5865_5869delinsGTCTA MANE Select ENSP00000233242.1:p.Val1955=
ENST00000616098.4:c.5865_5869delinsGTCTA ENSP00000477990.1:p.Val1955=
NM_000384.2:c.5865_5869delinsGTCTA NP_000375.2:p.Val1955=
XM_011532809.1:c.5864+1_5864+5delinsGTCTA XP_011531111.1:n.5864+1_5864+5delinsGTCTA
NM_000384.3:c.5865_5869delinsGTCTA MANE Select NP_000375.3:p.Val1955=
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