Canonical Allele Identifier: CA2661823207
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247593del , CM000664.2:g.169247593del GRCh38
NC_000002.11:g.170104103del , CM000664.1:g.170104103del GRCh37
NC_000002.10:g.169812349del NCBI36
NG_012634.1:g.120021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2771-77del MANE Select ENSP00000496870.1:n.2771-77del
ENST00000263816.7:c.2771-77del ENSP00000263816.3:n.2771-77del
ENST00000443831.1:c.2360-77del ENSP00000409813.1:n.2360-77del
NM_004525.2:c.2771-77del NP_004516.2:n.2771-77del
XM_011511183.1:c.2771-77del XP_011509485.1:n.2771-77del
XM_011511184.1:c.482-77del XP_011509486.1:n.482-77del
XM_011511185.1:c.2771-77del XP_011509487.1:n.2771-77del
NM_004525.3:c.2771-77del MANE Select NP_004516.2:n.2771-77del
XM_011511183.3:c.2771-77del XP_011509485.1:n.2771-77del
XM_011511184.2:c.482-77del XP_011509486.1:n.482-77del