Canonical Allele Identifier: CA2661823187
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247507dup , CM000664.2:g.169247507dup GRCh38
NC_000002.11:g.170104017dup , CM000664.1:g.170104017dup GRCh37
NC_000002.10:g.169812263dup NCBI36
NG_012634.1:g.120111dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2784dup MANE Select ENSP00000496870.1:p.Thr929TyrfsTer2
ENST00000263816.7:c.2784dup ENSP00000263816.3:p.Thr929TyrfsTer2
ENST00000443831.1:c.2373dup ENSP00000409813.1:p.Thr792TyrfsTer2
NM_004525.2:c.2784dup NP_004516.2:p.Thr929TyrfsTer2
XM_011511183.1:c.2784dup XP_011509485.1:p.Thr929TyrfsTer2
XM_011511184.1:c.495dup XP_011509486.1:p.Thr166TyrfsTer2
XM_011511185.1:c.2784dup XP_011509487.1:p.Thr929TyrfsTer2
NM_004525.3:c.2784dup MANE Select NP_004516.2:p.Thr929TyrfsTer2
XM_011511183.3:c.2784dup XP_011509485.1:p.Thr929TyrfsTer2
XM_011511184.2:c.495dup XP_011509486.1:p.Thr166TyrfsTer2