Canonical Allele Identifier: CA2661815125
Gene: LRP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2965283
ClinVar RCV Id: RCV003823449
gnomAD v4: 2-169154448-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154451dup , CM000664.2:g.169154451dup GRCh38
NC_000002.11:g.170010961dup , CM000664.1:g.170010961dup GRCh37
NC_000002.10:g.169719207dup NCBI36
NG_012634.1:g.213164dup

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+11dup MANE Select ENSP00000496870.1:n.12295+11dup
ENST00000649153.1:c.3195+11dup
ENST00000650252.1:c.1323+11dup ENSP00000496887.1:n.1323+11dup
ENST00000263816.7:c.12295+11dup ENSP00000263816.3:n.12295+11dup
NM_004525.2:c.12295+11dup NP_004516.2:n.12295+11dup
XM_011511183.1:c.12166+11dup XP_011509485.1:n.12166+11dup
XM_011511184.1:c.10006+11dup XP_011509486.1:n.10006+11dup
NM_004525.3:c.12295+11dup MANE Select NP_004516.2:n.12295+11dup
XM_011511183.3:c.12166+11dup XP_011509485.1:n.12166+11dup
XM_011511184.2:c.10006+11dup XP_011509486.1:n.10006+11dup
Search 100 bp 5'
Search 100 bp 3'