Canonical Allele Identifier: CA2753099782
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154380dup , CM000664.2:g.169154380dup GRCh38
NC_000002.11:g.170010890dup , CM000664.1:g.170010890dup GRCh37
NC_000002.10:g.169719136dup NCBI36
NG_012634.1:g.213234dup

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+81dup MANE Select ENSP00000496870.1:n.12295+81dup
ENST00000649153.1:c.3195+81dup
ENST00000650252.1:c.1323+81dup ENSP00000496887.1:n.1323+81dup
ENST00000263816.7:c.12295+81dup ENSP00000263816.3:n.12295+81dup
NM_004525.2:c.12295+81dup NP_004516.2:n.12295+81dup
XM_011511183.1:c.12166+81dup XP_011509485.1:n.12166+81dup
XM_011511184.1:c.10006+81dup XP_011509486.1:n.10006+81dup
NM_004525.3:c.12295+81dup MANE Select NP_004516.2:n.12295+81dup
XM_011511183.3:c.12166+81dup XP_011509485.1:n.12166+81dup
XM_011511184.2:c.10006+81dup XP_011509486.1:n.10006+81dup