Canonical Allele Identifier: CA349136914
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154463G>C , CM000664.2:g.169154463G>C GRCh38
NC_000002.11:g.170010973G>C , CM000664.1:g.170010973G>C GRCh37
NC_000002.10:g.169719219G>C NCBI36
NG_012634.1:g.213150C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12292C>G MANE Select ENSP00000496870.1:p.Leu4098Val
ENST00000649153.1:c.3192C>G
ENST00000650252.1:c.1320C>G ENSP00000496887.1:n.1320C>G
ENST00000263816.7:c.12292C>G ENSP00000263816.3:p.Leu4098Val
NM_004525.2:c.12292C>G NP_004516.2:p.Leu4098Val
XM_011511183.1:c.12163C>G XP_011509485.1:p.Leu4055Val
XM_011511184.1:c.10003C>G XP_011509486.1:p.Leu3335Val
NM_004525.3:c.12292C>G MANE Select NP_004516.2:p.Leu4098Val
XM_011511183.3:c.12163C>G XP_011509485.1:p.Leu4055Val
XM_011511184.2:c.10003C>G XP_011509486.1:p.Leu3335Val