Canonical Allele Identifier: CA2700664801

Gene: LRP1B

Linked Data

• dbSNP Id: rs2105317796

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963235_140963237del , CM000664.2:g.140963235_140963237del	GRCh38
NC_000002.11:g.141720804_141720806del , CM000664.1:g.141720804_141720806del	GRCh37
NC_000002.10:g.141437274_141437276del	NCBI36
NG_051023.1:g.1174229_1174231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11295_2888-11293del MANE Select	ENSP00000374135.3:n.2888-11295_2888-11293del
ENST00000389484.7:c.2888-11295_2888-11293del	ENSP00000374135.3:n.2888-11295_2888-11293del
ENST00000434794.1:c.323-11295_323-11293del	ENSP00000413239.1:n.323-11295_323-11293del
ENST00000618808.4:c.2546-11295_2546-11293del	ENSP00000478868.1:n.2546-11295_2546-11293del
NM_018557.2:c.2888-11295_2888-11293del	NP_061027.2:n.2888-11295_2888-11293del
XM_011511352.1:c.2999-11295_2999-11293del	XP_011509654.1:n.2999-11295_2999-11293del
XM_017004341.1:c.2498-11295_2498-11293del	XP_016859830.1:n.2498-11295_2498-11293del
XR_001738778.1:n.4622-11295_4622-11293del
NM_018557.3:c.2888-11295_2888-11293del MANE Select	NP_061027.2:n.2888-11295_2888-11293del