Canonical Allele Identifier: CA349137193
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154510T>C , CM000664.2:g.169154510T>C GRCh38
NC_000002.11:g.170011020T>C , CM000664.1:g.170011020T>C GRCh37
NC_000002.10:g.169719266T>C NCBI36
NG_012634.1:g.213103A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12245A>G MANE Select ENSP00000496870.1:p.Glu4082Gly
ENST00000649153.1:c.3145A>G
ENST00000650252.1:c.1273A>G ENSP00000496887.1:p.Asn425Asp
ENST00000263816.7:c.12245A>G ENSP00000263816.3:p.Glu4082Gly
NM_004525.2:c.12245A>G NP_004516.2:p.Glu4082Gly
XM_011511183.1:c.12116A>G XP_011509485.1:p.Glu4039Gly
XM_011511184.1:c.9956A>G XP_011509486.1:p.Glu3319Gly
NM_004525.3:c.12245A>G MANE Select NP_004516.2:p.Glu4082Gly
XM_011511183.3:c.12116A>G XP_011509485.1:p.Glu4039Gly
XM_011511184.2:c.9956A>G XP_011509486.1:p.Glu3319Gly