Canonical Allele Identifier: CA349136908
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154462A>G , CM000664.2:g.169154462A>G GRCh38
NC_000002.11:g.170010972A>G , CM000664.1:g.170010972A>G GRCh37
NC_000002.10:g.169719218A>G NCBI36
NG_012634.1:g.213151T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12293T>C MANE Select ENSP00000496870.1:p.Leu4098Pro
ENST00000649153.1:c.3193T>C
ENST00000650252.1:c.1321T>C ENSP00000496887.1:n.1321T>C
ENST00000263816.7:c.12293T>C ENSP00000263816.3:p.Leu4098Pro
NM_004525.2:c.12293T>C NP_004516.2:p.Leu4098Pro
XM_011511183.1:c.12164T>C XP_011509485.1:p.Leu4055Pro
XM_011511184.1:c.10004T>C XP_011509486.1:p.Leu3335Pro
NM_004525.3:c.12293T>C MANE Select NP_004516.2:p.Leu4098Pro
XM_011511183.3:c.12164T>C XP_011509485.1:p.Leu4055Pro
XM_011511184.2:c.10004T>C XP_011509486.1:p.Leu3335Pro