Canonical Allele Identifier: CA1293259413

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696098075

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963438_140963441del , CM000664.2:g.140963438_140963441del	GRCh38
NC_000002.11:g.141721007_141721010del , CM000664.1:g.141721007_141721010del	GRCh37
NC_000002.10:g.141437477_141437480del	NCBI36
NG_051023.1:g.1174023_1174026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11501_2888-11498del MANE Select	ENSP00000374135.3:n.2888-11501_2888-11498del
ENST00000389484.7:c.2888-11501_2888-11498del	ENSP00000374135.3:n.2888-11501_2888-11498del
ENST00000434794.1:c.323-11501_323-11498del	ENSP00000413239.1:n.323-11501_323-11498del
ENST00000618808.4:c.2546-11501_2546-11498del	ENSP00000478868.1:n.2546-11501_2546-11498del
NM_018557.2:c.2888-11501_2888-11498del	NP_061027.2:n.2888-11501_2888-11498del
XM_011511352.1:c.2999-11501_2999-11498del	XP_011509654.1:n.2999-11501_2999-11498del
XM_017004341.1:c.2498-11501_2498-11498del	XP_016859830.1:n.2498-11501_2498-11498del
XR_001738778.1:n.4622-11501_4622-11498del
NM_018557.3:c.2888-11501_2888-11498del MANE Select	NP_061027.2:n.2888-11501_2888-11498del