Canonical Allele Identifier: CA2658056809

Gene: APOB

Linked Data

• gnomAD v4: 2-21014940-TCCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014941_21014944del , CM000664.2:g.21014941_21014944del	GRCh38
NC_000002.11:g.21237813_21237816del , CM000664.1:g.21237813_21237816del	GRCh37
NC_000002.10:g.21091318_21091321del	NCBI36
NG_011793.1:g.34130_34133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+129_*3002+132del	ENSP00000501110.2:n.*3002+129_*3002+132del
ENST00000673882.2:c.*2791+129_*2791+132del	ENSP00000501253.2:n.*2791+129_*2791+132del
ENST00000673739.1:c.3410+129_3410+132del	ENSP00000501110.1:n.3410+129_3410+132del
ENST00000673882.1:c.3199+129_3199+132del	ENSP00000501253.1:n.3199+129_3199+132del
ENST00000233242.5:c.3696+129_3696+132del MANE Select	ENSP00000233242.1:n.3696+129_3696+132del
ENST00000616098.4:c.3696+129_3696+132del	ENSP00000477990.1:n.3696+129_3696+132del
NM_000384.2:c.3696+129_3696+132del	NP_000375.2:n.3696+129_3696+132del
XM_011532809.1:c.3696+129_3696+132del	XP_011531111.1:n.3696+129_3696+132del
NM_000384.3:c.3696+129_3696+132del MANE Select	NP_000375.3:n.3696+129_3696+132del