Canonical Allele Identifier: CA2749099710
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011050_21011051insACACATCTA , CM000664.2:g.21011050_21011051insACACATCTA GRCh38
NC_000002.11:g.21233922_21233923insACACATCTA , CM000664.1:g.21233922_21233923insACACATCTA GRCh37
NC_000002.10:g.21087427_21087428insACACATCTA NCBI36
NG_011793.1:g.38024_38025insAGATGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5818_5819insAGATGTGTT MANE Select ENSP00000233242.1:p.Phe1940Ter
ENST00000616098.4:c.5818_5819insAGATGTGTT ENSP00000477990.1:p.Phe1940Ter
NM_000384.2:c.5818_5819insAGATGTGTT NP_000375.2:p.Phe1940Ter
XM_011532809.1:c.5818_5819insAGATGTGTT XP_011531111.1:p.Phe1940Ter
NM_000384.3:c.5818_5819insAGATGTGTT MANE Select NP_000375.3:p.Phe1940Ter
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