Canonical Allele Identifier: CA2749099741

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014938_21014939insTTTTTTTTTTTTT , CM000664.2:g.21014938_21014939insTTTTTTTTTTTTT	GRCh38
NC_000002.11:g.21237810_21237811insTTTTTTTTTTTTT , CM000664.1:g.21237810_21237811insTTTTTTTTTTTTT	GRCh37
NC_000002.10:g.21091315_21091316insTTTTTTTTTTTTT	NCBI36
NG_011793.1:g.34144_34145insAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+143_*3002+144insAAAAAAAAAAAAA	ENSP00000501110.2:n.*3002+143_*3002+144insAAAAAAAAAAAAA
ENST00000673882.2:c.*2791+143_*2791+144insAAAAAAAAAAAAA	ENSP00000501253.2:n.*2791+143_*2791+144insAAAAAAAAAAAAA
ENST00000673739.1:c.3410+143_3410+144insAAAAAAAAAAAAA	ENSP00000501110.1:n.3410+143_3410+144insAAAAAAAAAAAAA
ENST00000673882.1:c.3199+143_3199+144insAAAAAAAAAAAAA	ENSP00000501253.1:n.3199+143_3199+144insAAAAAAAAAAAAA
ENST00000233242.5:c.3696+143_3696+144insAAAAAAAAAAAAA MANE Select	ENSP00000233242.1:n.3696+143_3696+144insAAAAAAAAAAAAA
ENST00000616098.4:c.3696+143_3696+144insAAAAAAAAAAAAA	ENSP00000477990.1:n.3696+143_3696+144insAAAAAAAAAAAAA
NM_000384.2:c.3696+143_3696+144insAAAAAAAAAAAAA	NP_000375.2:n.3696+143_3696+144insAAAAAAAAAAAAA
XM_011532809.1:c.3696+143_3696+144insAAAAAAAAAAAAA	XP_011531111.1:n.3696+143_3696+144insAAAAAAAAAAAAA
NM_000384.3:c.3696+143_3696+144insAAAAAAAAAAAAA MANE Select	NP_000375.3:n.3696+143_3696+144insAAAAAAAAAAAAA