Canonical Allele Identifier: CA1028210402

Gene: APOB

Linked Data

• gnomAD v3: 2-21038334-C-CTTTT
• gnomAD v4: 2-21038334-C-CTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038337_21038340dup , CM000664.2:g.21038337_21038340dup	GRCh38
NC_000002.11:g.21261209_21261212dup , CM000664.1:g.21261209_21261212dup	GRCh37
NC_000002.10:g.21114714_21114717dup	NCBI36
NG_011793.1:g.10736_10739dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1083_384-1080dup	ENSP00000501110.2:n.384-1083_384-1080dup
ENST00000673882.2:c.384-1083_384-1080dup	ENSP00000501253.2:n.384-1083_384-1080dup
ENST00000673739.1:c.252-1083_252-1080dup	ENSP00000501110.1:n.252-1083_252-1080dup
ENST00000673882.1:c.252-1083_252-1080dup	ENSP00000501253.1:n.252-1083_252-1080dup
ENST00000233242.5:c.384-227_384-224dup MANE Select	ENSP00000233242.1:n.384-227_384-224dup
ENST00000399256.4:c.384-227_384-224dup	ENSP00000382200.4:n.384-227_384-224dup
ENST00000616098.4:c.384-227_384-224dup	ENSP00000477990.1:n.384-227_384-224dup
NM_000384.2:c.384-227_384-224dup	NP_000375.2:n.384-227_384-224dup
XM_011532809.1:c.384-227_384-224dup	XP_011531111.1:n.384-227_384-224dup
NM_000384.3:c.384-227_384-224dup MANE Select	NP_000375.3:n.384-227_384-224dup