Canonical Allele Identifier: CA1293259247

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963289_140963292delinsAAAG , CM000664.2:g.140963289_140963292delinsAAAG	GRCh38
NC_000002.11:g.141720858_141720861delinsAAAG , CM000664.1:g.141720858_141720861delinsAAAG	GRCh37
NC_000002.10:g.141437328_141437331delinsAAAG	NCBI36
NG_051023.1:g.1174172_1174175delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11352_2888-11349delinsCTTT MANE Select	ENSP00000374135.3:n.2888-11352_2888-11349delinsCTTT
ENST00000389484.7:c.2888-11352_2888-11349delinsCTTT	ENSP00000374135.3:n.2888-11352_2888-11349delinsCTTT
ENST00000434794.1:c.323-11352_323-11349delinsCTTT	ENSP00000413239.1:n.323-11352_323-11349delinsCTTT
ENST00000618808.4:c.2546-11352_2546-11349delinsCTTT	ENSP00000478868.1:n.2546-11352_2546-11349delinsCTTT
NM_018557.2:c.2888-11352_2888-11349delinsCTTT	NP_061027.2:n.2888-11352_2888-11349delinsCTTT
XM_011511352.1:c.2999-11352_2999-11349delinsCTTT	XP_011509654.1:n.2999-11352_2999-11349delinsCTTT
XM_017004341.1:c.2498-11352_2498-11349delinsCTTT	XP_016859830.1:n.2498-11352_2498-11349delinsCTTT
XR_001738778.1:n.4622-11352_4622-11349delinsCTTT
NM_018557.3:c.2888-11352_2888-11349delinsCTTT MANE Select	NP_061027.2:n.2888-11352_2888-11349delinsCTTT