Canonical Allele Identifier: CA349136962
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154471T>C , CM000664.2:g.169154471T>C GRCh38
NC_000002.11:g.170010981T>C , CM000664.1:g.170010981T>C GRCh37
NC_000002.10:g.169719227T>C NCBI36
NG_012634.1:g.213142A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12284A>G MANE Select ENSP00000496870.1:p.Asp4095Gly
ENST00000649153.1:c.3184A>G
ENST00000650252.1:c.1312A>G ENSP00000496887.1:p.Thr438Ala
ENST00000263816.7:c.12284A>G ENSP00000263816.3:p.Asp4095Gly
NM_004525.2:c.12284A>G NP_004516.2:p.Asp4095Gly
XM_011511183.1:c.12155A>G XP_011509485.1:p.Asp4052Gly
XM_011511184.1:c.9995A>G XP_011509486.1:p.Asp3332Gly
NM_004525.3:c.12284A>G MANE Select NP_004516.2:p.Asp4095Gly
XM_011511183.3:c.12155A>G XP_011509485.1:p.Asp4052Gly
XM_011511184.2:c.9995A>G XP_011509486.1:p.Asp3332Gly