Canonical Allele Identifier: CA2658056794

Gene: APOB

Linked Data

• gnomAD v4: 2-21014929-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014936_21014938dup , CM000664.2:g.21014936_21014938dup	GRCh38
NC_000002.11:g.21237808_21237810dup , CM000664.1:g.21237808_21237810dup	GRCh37
NC_000002.10:g.21091313_21091315dup	NCBI36
NG_011793.1:g.34142_34144dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+141_*3002+143dup	ENSP00000501110.2:n.*3002+141_*3002+143dup
ENST00000673882.2:c.*2791+141_*2791+143dup	ENSP00000501253.2:n.*2791+141_*2791+143dup
ENST00000673739.1:c.3410+141_3410+143dup	ENSP00000501110.1:n.3410+141_3410+143dup
ENST00000673882.1:c.3199+141_3199+143dup	ENSP00000501253.1:n.3199+141_3199+143dup
ENST00000233242.5:c.3696+141_3696+143dup MANE Select	ENSP00000233242.1:n.3696+141_3696+143dup
ENST00000616098.4:c.3696+141_3696+143dup	ENSP00000477990.1:n.3696+141_3696+143dup
NM_000384.2:c.3696+141_3696+143dup	NP_000375.2:n.3696+141_3696+143dup
XM_011532809.1:c.3696+141_3696+143dup	XP_011531111.1:n.3696+141_3696+143dup
NM_000384.3:c.3696+141_3696+143dup MANE Select	NP_000375.3:n.3696+141_3696+143dup