Canonical Allele Identifier: CA349136978
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154474T>A , CM000664.2:g.169154474T>A GRCh38
NC_000002.11:g.170010984T>A , CM000664.1:g.170010984T>A GRCh37
NC_000002.10:g.169719230T>A NCBI36
NG_012634.1:g.213139A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12281A>T MANE Select ENSP00000496870.1:p.Lys4094Met
ENST00000649153.1:c.3181A>T
ENST00000650252.1:c.1309A>T ENSP00000496887.1:p.Arg437Trp
ENST00000263816.7:c.12281A>T ENSP00000263816.3:p.Lys4094Met
NM_004525.2:c.12281A>T NP_004516.2:p.Lys4094Met
XM_011511183.1:c.12152A>T XP_011509485.1:p.Lys4051Met
XM_011511184.1:c.9992A>T XP_011509486.1:p.Lys3331Met
NM_004525.3:c.12281A>T MANE Select NP_004516.2:p.Lys4094Met
XM_011511183.3:c.12152A>T XP_011509485.1:p.Lys4051Met
XM_011511184.2:c.9992A>T XP_011509486.1:p.Lys3331Met