Canonical Allele Identifier: CA1306353859
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259341_169259342delinsTC , CM000664.2:g.169259341_169259342delinsTC GRCh38
NC_000002.11:g.170115851_170115852delinsTC , CM000664.1:g.170115851_170115852delinsTC GRCh37
NC_000002.10:g.169824097_169824098delinsTC NCBI36
NG_012634.1:g.108271_108272delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-125_2321-124delinsGA MANE Select ENSP00000496870.1:n.2321-125_2321-124delinsGA
ENST00000263816.7:c.2321-125_2321-124delinsGA ENSP00000263816.3:n.2321-125_2321-124delinsGA
ENST00000443831.1:c.1910-125_1910-124delinsGA ENSP00000409813.1:n.1910-125_1910-124delinsGA
NM_004525.2:c.2321-125_2321-124delinsGA NP_004516.2:n.2321-125_2321-124delinsGA
XM_011511183.1:c.2321-125_2321-124delinsGA XP_011509485.1:n.2321-125_2321-124delinsGA
XM_011511184.1:c.32-125_32-124delinsGA XP_011509486.1:n.32-125_32-124delinsGA
XM_011511185.1:c.2321-125_2321-124delinsGA XP_011509487.1:n.2321-125_2321-124delinsGA
NM_004525.3:c.2321-125_2321-124delinsGA MANE Select NP_004516.2:n.2321-125_2321-124delinsGA
XM_011511183.3:c.2321-125_2321-124delinsGA XP_011509485.1:n.2321-125_2321-124delinsGA
XM_011511184.2:c.32-125_32-124delinsGA XP_011509486.1:n.32-125_32-124delinsGA