Canonical Allele Identifier: CA349137046
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154484A>T , CM000664.2:g.169154484A>T GRCh38
NC_000002.11:g.170010994A>T , CM000664.1:g.170010994A>T GRCh37
NC_000002.10:g.169719240A>T NCBI36
NG_012634.1:g.213129T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12271T>A MANE Select ENSP00000496870.1:p.Trp4091Arg
ENST00000649153.1:c.3171T>A
ENST00000650252.1:c.1299T>A ENSP00000496887.1:p.Ile433=
ENST00000263816.7:c.12271T>A ENSP00000263816.3:p.Trp4091Arg
NM_004525.2:c.12271T>A NP_004516.2:p.Trp4091Arg
XM_011511183.1:c.12142T>A XP_011509485.1:p.Trp4048Arg
XM_011511184.1:c.9982T>A XP_011509486.1:p.Trp3328Arg
NM_004525.3:c.12271T>A MANE Select NP_004516.2:p.Trp4091Arg
XM_011511183.3:c.12142T>A XP_011509485.1:p.Trp4048Arg
XM_011511184.2:c.9982T>A XP_011509486.1:p.Trp3328Arg