Canonical Allele Identifier: CA2749099742

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014944_21014945insTTTTT , CM000664.2:g.21014944_21014945insTTTTT	GRCh38
NC_000002.11:g.21237816_21237817insTTTTT , CM000664.1:g.21237816_21237817insTTTTT	GRCh37
NC_000002.10:g.21091321_21091322insTTTTT	NCBI36
NG_011793.1:g.34129_34130insAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+128_*3002+129insAAAAA	ENSP00000501110.2:n.*3002+128_*3002+129insAAAAA
ENST00000673882.2:c.*2791+128_*2791+129insAAAAA	ENSP00000501253.2:n.*2791+128_*2791+129insAAAAA
ENST00000673739.1:c.3410+128_3410+129insAAAAA	ENSP00000501110.1:n.3410+128_3410+129insAAAAA
ENST00000673882.1:c.3199+128_3199+129insAAAAA	ENSP00000501253.1:n.3199+128_3199+129insAAAAA
ENST00000233242.5:c.3696+128_3696+129insAAAAA MANE Select	ENSP00000233242.1:n.3696+128_3696+129insAAAAA
ENST00000616098.4:c.3696+128_3696+129insAAAAA	ENSP00000477990.1:n.3696+128_3696+129insAAAAA
NM_000384.2:c.3696+128_3696+129insAAAAA	NP_000375.2:n.3696+128_3696+129insAAAAA
XM_011532809.1:c.3696+128_3696+129insAAAAA	XP_011531111.1:n.3696+128_3696+129insAAAAA
NM_000384.3:c.3696+128_3696+129insAAAAA MANE Select	NP_000375.3:n.3696+128_3696+129insAAAAA