Canonical Allele Identifier: CA2577149100
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154384del , CM000664.2:g.169154384del GRCh38
NC_000002.11:g.170010894del , CM000664.1:g.170010894del GRCh37
NC_000002.10:g.169719140del NCBI36
NG_012634.1:g.213231del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12295+78del MANE Select ENSP00000496870.1:n.12295+78del
ENST00000649153.1:c.3195+78del
ENST00000650252.1:c.1323+78del ENSP00000496887.1:n.1323+78del
ENST00000263816.7:c.12295+78del ENSP00000263816.3:n.12295+78del
NM_004525.2:c.12295+78del NP_004516.2:n.12295+78del
XM_011511183.1:c.12166+78del XP_011509485.1:n.12166+78del
XM_011511184.1:c.10006+78del XP_011509486.1:n.10006+78del
NM_004525.3:c.12295+78del MANE Select NP_004516.2:n.12295+78del
XM_011511183.3:c.12166+78del XP_011509485.1:n.12166+78del
XM_011511184.2:c.10006+78del XP_011509486.1:n.10006+78del