Canonical Allele Identifier: CA1293259454
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1696099243

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963445_140963447del , CM000664.2:g.140963445_140963447del GRCh38
NC_000002.11:g.141721014_141721016del , CM000664.1:g.141721014_141721016del GRCh37
NC_000002.10:g.141437484_141437486del NCBI36
NG_051023.1:g.1174017_1174019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11507_2888-11505del MANE Select ENSP00000374135.3:n.2888-11507_2888-11505del
ENST00000389484.7:c.2888-11507_2888-11505del ENSP00000374135.3:n.2888-11507_2888-11505del
ENST00000434794.1:c.323-11507_323-11505del ENSP00000413239.1:n.323-11507_323-11505del
ENST00000618808.4:c.2546-11507_2546-11505del ENSP00000478868.1:n.2546-11507_2546-11505del
NM_018557.2:c.2888-11507_2888-11505del NP_061027.2:n.2888-11507_2888-11505del
XM_011511352.1:c.2999-11507_2999-11505del XP_011509654.1:n.2999-11507_2999-11505del
XM_017004341.1:c.2498-11507_2498-11505del XP_016859830.1:n.2498-11507_2498-11505del
XR_001738778.1:n.4622-11507_4622-11505del
NM_018557.3:c.2888-11507_2888-11505del MANE Select NP_061027.2:n.2888-11507_2888-11505del