Canonical Allele Identifier: CA2658048654

Gene: APOB

Linked Data

• gnomAD v4: 2-21028282-GCTCAGGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028288_21028296del , CM000664.2:g.21028288_21028296del	GRCh38
NC_000002.11:g.21251160_21251168del , CM000664.1:g.21251160_21251168del	GRCh37
NC_000002.10:g.21104665_21104673del	NCBI36
NG_011793.1:g.20783_20791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1135+36_*1135+44del	ENSP00000501110.2:n.*1135+36_*1135+44del
ENST00000673882.2:c.*1135+36_*1135+44del	ENSP00000501253.2:n.*1135+36_*1135+44del
ENST00000673739.1:c.1543+36_1543+44del	ENSP00000501110.1:n.1543+36_1543+44del
ENST00000673882.1:c.1543+36_1543+44del	ENSP00000501253.1:n.1543+36_1543+44del
ENST00000233242.5:c.1829+36_1829+44del MANE Select	ENSP00000233242.1:n.1829+36_1829+44del
ENST00000399256.4:c.1829+36_1829+44del	ENSP00000382200.4:n.1829+36_1829+44del
ENST00000616098.4:c.1829+36_1829+44del	ENSP00000477990.1:n.1829+36_1829+44del
NM_000384.2:c.1829+36_1829+44del	NP_000375.2:n.1829+36_1829+44del
XM_011532809.1:c.1829+36_1829+44del	XP_011531111.1:n.1829+36_1829+44del
NM_000384.3:c.1829+36_1829+44del MANE Select	NP_000375.3:n.1829+36_1829+44del