Canonical Allele Identifier: CA349137030
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs2105358831

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154481C>T , CM000664.2:g.169154481C>T GRCh38
NC_000002.11:g.170010991C>T , CM000664.1:g.170010991C>T GRCh37
NC_000002.10:g.169719237C>T NCBI36
NG_012634.1:g.213132G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12274G>A MANE Select ENSP00000496870.1:p.Asp4092Asn
ENST00000649153.1:c.3174G>A
ENST00000650252.1:c.1302G>A ENSP00000496887.1:p.Gly434=
ENST00000263816.7:c.12274G>A ENSP00000263816.3:p.Asp4092Asn
NM_004525.2:c.12274G>A NP_004516.2:p.Asp4092Asn
XM_011511183.1:c.12145G>A XP_011509485.1:p.Asp4049Asn
XM_011511184.1:c.9985G>A XP_011509486.1:p.Asp3329Asn
NM_004525.3:c.12274G>A MANE Select NP_004516.2:p.Asp4092Asn
XM_011511183.3:c.12145G>A XP_011509485.1:p.Asp4049Asn
XM_011511184.2:c.9985G>A XP_011509486.1:p.Asp3329Asn