Canonical Allele Identifier: CA2753102789
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259317_169259319del , CM000664.2:g.169259317_169259319del GRCh38
NC_000002.11:g.170115827_170115829del , CM000664.1:g.170115827_170115829del GRCh37
NC_000002.10:g.169824073_169824075del NCBI36
NG_012634.1:g.108294_108296del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-102_2321-100del MANE Select ENSP00000496870.1:n.2321-102_2321-100del
ENST00000263816.7:c.2321-102_2321-100del ENSP00000263816.3:n.2321-102_2321-100del
ENST00000443831.1:c.1910-102_1910-100del ENSP00000409813.1:n.1910-102_1910-100del
NM_004525.2:c.2321-102_2321-100del NP_004516.2:n.2321-102_2321-100del
XM_011511183.1:c.2321-102_2321-100del XP_011509485.1:n.2321-102_2321-100del
XM_011511184.1:c.32-102_32-100del XP_011509486.1:n.32-102_32-100del
XM_011511185.1:c.2321-102_2321-100del XP_011509487.1:n.2321-102_2321-100del
NM_004525.3:c.2321-102_2321-100del MANE Select NP_004516.2:n.2321-102_2321-100del
XM_011511183.3:c.2321-102_2321-100del XP_011509485.1:n.2321-102_2321-100del
XM_011511184.2:c.32-102_32-100del XP_011509486.1:n.32-102_32-100del