Canonical Allele Identifier: CA349137041
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154483C>G , CM000664.2:g.169154483C>G GRCh38
NC_000002.11:g.170010993C>G , CM000664.1:g.170010993C>G GRCh37
NC_000002.10:g.169719239C>G NCBI36
NG_012634.1:g.213130G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12272G>C MANE Select ENSP00000496870.1:p.Trp4091Ser
ENST00000649153.1:c.3172G>C
ENST00000650252.1:c.1300G>C ENSP00000496887.1:p.Gly434Arg
ENST00000263816.7:c.12272G>C ENSP00000263816.3:p.Trp4091Ser
NM_004525.2:c.12272G>C NP_004516.2:p.Trp4091Ser
XM_011511183.1:c.12143G>C XP_011509485.1:p.Trp4048Ser
XM_011511184.1:c.9983G>C XP_011509486.1:p.Trp3328Ser
NM_004525.3:c.12272G>C MANE Select NP_004516.2:p.Trp4091Ser
XM_011511183.3:c.12143G>C XP_011509485.1:p.Trp4048Ser
XM_011511184.2:c.9983G>C XP_011509486.1:p.Trp3328Ser