Canonical Allele Identifier: CA646545187

Gene: APOB

Linked Data

• COSMIC: COSN20080688

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014928_21014929insT , CM000664.2:g.21014928_21014929insT	GRCh38
NC_000002.11:g.21237800_21237801insT , CM000664.1:g.21237800_21237801insT	GRCh37
NC_000002.10:g.21091305_21091306insT	NCBI36
NG_011793.1:g.34145_34146insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+144_*3002+145insA	ENSP00000501110.2:n.*3002+144_*3002+145insA
ENST00000673882.2:c.*2791+144_*2791+145insA	ENSP00000501253.2:n.*2791+144_*2791+145insA
ENST00000673739.1:c.3410+144_3410+145insA	ENSP00000501110.1:n.3410+144_3410+145insA
ENST00000673882.1:c.3199+144_3199+145insA	ENSP00000501253.1:n.3199+144_3199+145insA
ENST00000233242.5:c.3696+144_3696+145insA MANE Select	ENSP00000233242.1:n.3696+144_3696+145insA
ENST00000616098.4:c.3696+144_3696+145insA	ENSP00000477990.1:n.3696+144_3696+145insA
NM_000384.2:c.3696+144_3696+145insA	NP_000375.2:n.3696+144_3696+145insA
XM_011532809.1:c.3696+144_3696+145insA	XP_011531111.1:n.3696+144_3696+145insA
NM_000384.3:c.3696+144_3696+145insA MANE Select	NP_000375.3:n.3696+144_3696+145insA