Canonical Allele Identifier: CA2493478794

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014929_21014931delinsGTT , CM000664.2:g.21014929_21014931delinsGTT	GRCh38
NC_000002.11:g.21237801_21237803delinsGTT , CM000664.1:g.21237801_21237803delinsGTT	GRCh37
NC_000002.10:g.21091306_21091308delinsGTT	NCBI36
NG_011793.1:g.34143_34145delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+142_*3002+144delinsAAC	ENSP00000501110.2:n.*3002+142_*3002+144delinsAAC
ENST00000673882.2:c.*2791+142_*2791+144delinsAAC	ENSP00000501253.2:n.*2791+142_*2791+144delinsAAC
ENST00000673739.1:c.3410+142_3410+144delinsAAC	ENSP00000501110.1:n.3410+142_3410+144delinsAAC
ENST00000673882.1:c.3199+142_3199+144delinsAAC	ENSP00000501253.1:n.3199+142_3199+144delinsAAC
ENST00000233242.5:c.3696+142_3696+144delinsAAC MANE Select	ENSP00000233242.1:n.3696+142_3696+144delinsAAC
ENST00000616098.4:c.3696+142_3696+144delinsAAC	ENSP00000477990.1:n.3696+142_3696+144delinsAAC
NM_000384.2:c.3696+142_3696+144delinsAAC	NP_000375.2:n.3696+142_3696+144delinsAAC
XM_011532809.1:c.3696+142_3696+144delinsAAC	XP_011531111.1:n.3696+142_3696+144delinsAAC
NM_000384.3:c.3696+142_3696+144delinsAAC MANE Select	NP_000375.3:n.3696+142_3696+144delinsAAC