Canonical Allele Identifier: CA2493472827
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002171_21002173delinsAGC , CM000664.2:g.21002171_21002173delinsAGC GRCh38
NC_000002.11:g.21225043_21225045delinsAGC , CM000664.1:g.21225043_21225045delinsAGC GRCh37
NC_000002.10:g.21078548_21078550delinsAGC NCBI36
NG_011793.1:g.46901_46903delinsGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.13249_13251delinsGCT MANE Select ENSP00000233242.1:p.Ala4417=
ENST00000616098.4:c.13247_13249delinsGCT ENSP00000477990.1:n.13247_13249delinsGCT
NM_000384.2:c.13249_13251delinsGCT NP_000375.2:p.Ala4417=
XM_011532809.1:c.5870-2900_5870-2898delinsGCT XP_011531111.1:n.5870-2900_5870-2898delin...
NM_000384.3:c.13249_13251delinsGCT MANE Select NP_000375.3:p.Ala4417=