Canonical Allele Identifier: CA2569270198

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021177_21021178insAACCAGTTTAGAAATCTAGCTGTCAAATAGACCTATGGAT , CM000664.2:g.21021177_21021178insAACCAGTTTAGAAATCTAGCTGTCAAATAGACCTATGGAT	GRCh38
NC_000002.11:g.21244049_21244050insAACCAGTTTAGAAATCTAGCTGTCAAATAGACCTATGGAT , CM000664.1:g.21244049_21244050insAACCAGTTTAGAAATCTAGCTGTCAAATAGACCTATGGAT	GRCh37
NC_000002.10:g.21097554_21097555insAACCAGTTTAGAAATCTAGCTGTCAAATAGACCTATGGAT	NCBI36
NG_011793.1:g.27896_27897insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2123-1273_*2123-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	ENSP00000501110.2:n.*2123-1273_*2123-1272insATCCATAGGTCTATTTG...
ENST00000673882.2:c.*2123-1273_*2123-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	ENSP00000501253.2:n.*2123-1273_*2123-1272insATCCATAGGTCTATTTG...
ENST00000673739.1:c.2531-1273_2531-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	ENSP00000501110.1:n.2531-1273_2531-1272insATCCATAGGTCTATTTGAC...
ENST00000673882.1:c.2531-1273_2531-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	ENSP00000501253.1:n.2531-1273_2531-1272insATCCATAGGTCTATTTGAC...
ENST00000233242.5:c.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT MANE Select	ENSP00000233242.1:n.2817-1273_2817-1272insATCCATAGGTCTATTTGAC...
ENST00000616098.4:c.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	ENSP00000477990.1:n.2817-1273_2817-1272insATCCATAGGTCTATTTGAC...
NM_000384.2:c.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	NP_000375.2:n.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAG...
XM_011532809.1:c.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT	XP_011531111.1:n.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGC...
NM_000384.3:c.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAGATTTCTAAACTGGTT MANE Select	NP_000375.3:n.2817-1273_2817-1272insATCCATAGGTCTATTTGACAGCTAG...