Canonical Allele Identifier: CA59921105
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs372272914

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259170C>T , CM000664.2:g.169259170C>T GRCh38
NC_000002.11:g.170115680C>T , CM000664.1:g.170115680C>T GRCh37
NC_000002.10:g.169823926C>T NCBI36
NG_012634.1:g.108443G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2368G>A MANE Select ENSP00000496870.1:p.Ala790Thr
ENST00000263816.7:c.2368G>A ENSP00000263816.3:p.Ala790Thr
ENST00000443831.1:c.1957G>A ENSP00000409813.1:p.Ala653Thr
NM_004525.2:c.2368G>A NP_004516.2:p.Ala790Thr
XM_011511183.1:c.2368G>A XP_011509485.1:p.Ala790Thr
XM_011511184.1:c.79G>A XP_011509486.1:p.Ala27Thr
XM_011511185.1:c.2368G>A XP_011509487.1:p.Ala790Thr
NM_004525.3:c.2368G>A MANE Select NP_004516.2:p.Ala790Thr
XM_011511183.3:c.2368G>A XP_011509485.1:p.Ala790Thr
XM_011511184.2:c.79G>A XP_011509486.1:p.Ala27Thr