Canonical Allele Identifier: CA2749099743

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014945_21014946insTTTTTTT , CM000664.2:g.21014945_21014946insTTTTTTT	GRCh38
NC_000002.11:g.21237817_21237818insTTTTTTT , CM000664.1:g.21237817_21237818insTTTTTTT	GRCh37
NC_000002.10:g.21091322_21091323insTTTTTTT	NCBI36
NG_011793.1:g.34128_34129insAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+127_*3002+128insAAAAAAA	ENSP00000501110.2:n.*3002+127_*3002+128insAAAAAAA
ENST00000673882.2:c.*2791+127_*2791+128insAAAAAAA	ENSP00000501253.2:n.*2791+127_*2791+128insAAAAAAA
ENST00000673739.1:c.3410+127_3410+128insAAAAAAA	ENSP00000501110.1:n.3410+127_3410+128insAAAAAAA
ENST00000673882.1:c.3199+127_3199+128insAAAAAAA	ENSP00000501253.1:n.3199+127_3199+128insAAAAAAA
ENST00000233242.5:c.3696+127_3696+128insAAAAAAA MANE Select	ENSP00000233242.1:n.3696+127_3696+128insAAAAAAA
ENST00000616098.4:c.3696+127_3696+128insAAAAAAA	ENSP00000477990.1:n.3696+127_3696+128insAAAAAAA
NM_000384.2:c.3696+127_3696+128insAAAAAAA	NP_000375.2:n.3696+127_3696+128insAAAAAAA
XM_011532809.1:c.3696+127_3696+128insAAAAAAA	XP_011531111.1:n.3696+127_3696+128insAAAAAAA
NM_000384.3:c.3696+127_3696+128insAAAAAAA MANE Select	NP_000375.3:n.3696+127_3696+128insAAAAAAA