Canonical Allele Identifier: CA1293259434

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696098652

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963444_140963445insTTAT , CM000664.2:g.140963444_140963445insTTAT	GRCh38
NC_000002.11:g.141721013_141721014insTTAT , CM000664.1:g.141721013_141721014insTTAT	GRCh37
NC_000002.10:g.141437483_141437484insTTAT	NCBI36
NG_051023.1:g.1174020_1174021insTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11504_2888-11503insTAAA MANE Select	ENSP00000374135.3:n.2888-11504_2888-11503insTAAA
ENST00000389484.7:c.2888-11504_2888-11503insTAAA	ENSP00000374135.3:n.2888-11504_2888-11503insTAAA
ENST00000434794.1:c.323-11504_323-11503insTAAA	ENSP00000413239.1:n.323-11504_323-11503insTAAA
ENST00000618808.4:c.2546-11504_2546-11503insTAAA	ENSP00000478868.1:n.2546-11504_2546-11503insTAAA
NM_018557.2:c.2888-11504_2888-11503insTAAA	NP_061027.2:n.2888-11504_2888-11503insTAAA
XM_011511352.1:c.2999-11504_2999-11503insTAAA	XP_011509654.1:n.2999-11504_2999-11503insTAAA
XM_017004341.1:c.2498-11504_2498-11503insTAAA	XP_016859830.1:n.2498-11504_2498-11503insTAAA
XR_001738778.1:n.4622-11504_4622-11503insTAAA
NM_018557.3:c.2888-11504_2888-11503insTAAA MANE Select	NP_061027.2:n.2888-11504_2888-11503insTAAA