Canonical Allele Identifier: CA349136968
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154472C>A , CM000664.2:g.169154472C>A GRCh38
NC_000002.11:g.170010982C>A , CM000664.1:g.170010982C>A GRCh37
NC_000002.10:g.169719228C>A NCBI36
NG_012634.1:g.213141G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12283G>T MANE Select ENSP00000496870.1:p.Asp4095Tyr
ENST00000649153.1:c.3183G>T
ENST00000650252.1:c.1311G>T ENSP00000496887.1:p.Arg437Ser
ENST00000263816.7:c.12283G>T ENSP00000263816.3:p.Asp4095Tyr
NM_004525.2:c.12283G>T NP_004516.2:p.Asp4095Tyr
XM_011511183.1:c.12154G>T XP_011509485.1:p.Asp4052Tyr
XM_011511184.1:c.9994G>T XP_011509486.1:p.Asp3332Tyr
NM_004525.3:c.12283G>T MANE Select NP_004516.2:p.Asp4095Tyr
XM_011511183.3:c.12154G>T XP_011509485.1:p.Asp4052Tyr
XM_011511184.2:c.9994G>T XP_011509486.1:p.Asp3332Tyr