Canonical Allele Identifier: CA59898001
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs535009810

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154373_169154375del , CM000664.2:g.169154373_169154375del GRCh38
NC_000002.11:g.170010883_170010885del , CM000664.1:g.170010883_170010885del GRCh37
NC_000002.10:g.169719129_169719131del NCBI36
NG_012634.1:g.213239_213241del

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+86_12295+88del MANE Select ENSP00000496870.1:n.12295+86_12295+88del
ENST00000649153.1:c.3195+86_3195+88del
ENST00000650252.1:c.1323+86_1323+88del ENSP00000496887.1:n.1323+86_1323+88del
ENST00000263816.7:c.12295+86_12295+88del ENSP00000263816.3:n.12295+86_12295+88del
NM_004525.2:c.12295+86_12295+88del NP_004516.2:n.12295+86_12295+88del
XM_011511183.1:c.12166+86_12166+88del XP_011509485.1:n.12166+86_12166+88del
XM_011511184.1:c.10006+86_10006+88del XP_011509486.1:n.10006+86_10006+88del
NM_004525.3:c.12295+86_12295+88del MANE Select NP_004516.2:n.12295+86_12295+88del
XM_011511183.3:c.12166+86_12166+88del XP_011509485.1:n.12166+86_12166+88del
XM_011511184.2:c.10006+86_10006+88del XP_011509486.1:n.10006+86_10006+88del