Canonical Allele Identifier: CA349147688
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169128699G>C , CM000664.2:g.169128699G>C GRCh38
NC_000002.11:g.169985209G>C , CM000664.1:g.169985209G>C GRCh37
NC_000002.10:g.169693455G>C NCBI36
NG_012634.1:g.238914C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13932C>G MANE Select ENSP00000496870.1:p.Asp4644Glu
ENST00000649153.1:c.4741C>G
ENST00000650252.1:c.2923C>G ENSP00000496887.1:n.2923C>G
ENST00000263816.7:c.13932C>G ENSP00000263816.3:p.Asp4644Glu
NM_004525.2:c.13932C>G NP_004516.2:p.Asp4644Glu
XM_011511183.1:c.13803C>G XP_011509485.1:p.Asp4601Glu
XM_011511184.1:c.11643C>G XP_011509486.1:p.Asp3881Glu
NM_004525.3:c.13932C>G MANE Select NP_004516.2:p.Asp4644Glu
XM_011511183.3:c.13803C>G XP_011509485.1:p.Asp4601Glu
XM_011511184.2:c.11643C>G XP_011509486.1:p.Asp3881Glu