Canonical Allele Identifier: CA2752441300

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963461_140963462insATATA , CM000664.2:g.140963461_140963462insATATA	GRCh38
NC_000002.11:g.141721030_141721031insATATA , CM000664.1:g.141721030_141721031insATATA	GRCh37
NC_000002.10:g.141437500_141437501insATATA	NCBI36
NG_051023.1:g.1174002_1174003insTATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11522_2888-11521insTATAT MANE Select	ENSP00000374135.3:n.2888-11522_2888-11521insTATAT
ENST00000389484.7:c.2888-11522_2888-11521insTATAT	ENSP00000374135.3:n.2888-11522_2888-11521insTATAT
ENST00000434794.1:c.323-11522_323-11521insTATAT	ENSP00000413239.1:n.323-11522_323-11521insTATAT
ENST00000618808.4:c.2546-11522_2546-11521insTATAT	ENSP00000478868.1:n.2546-11522_2546-11521insTATAT
NM_018557.2:c.2888-11522_2888-11521insTATAT	NP_061027.2:n.2888-11522_2888-11521insTATAT
XM_011511352.1:c.2999-11522_2999-11521insTATAT	XP_011509654.1:n.2999-11522_2999-11521insTATAT
XM_017004341.1:c.2498-11522_2498-11521insTATAT	XP_016859830.1:n.2498-11522_2498-11521insTATAT
XR_001738778.1:n.4622-11522_4622-11521insTATAT
NM_018557.3:c.2888-11522_2888-11521insTATAT MANE Select	NP_061027.2:n.2888-11522_2888-11521insTATAT