Canonical Allele Identifier: CA349136946
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154468A>T , CM000664.2:g.169154468A>T GRCh38
NC_000002.11:g.170010978A>T , CM000664.1:g.170010978A>T GRCh37
NC_000002.10:g.169719224A>T NCBI36
NG_012634.1:g.213145T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12287T>A MANE Select ENSP00000496870.1:p.Ile4096Lys
ENST00000649153.1:c.3187T>A
ENST00000650252.1:c.1315T>A ENSP00000496887.1:p.Ter439Lys
ENST00000263816.7:c.12287T>A ENSP00000263816.3:p.Ile4096Lys
NM_004525.2:c.12287T>A NP_004516.2:p.Ile4096Lys
XM_011511183.1:c.12158T>A XP_011509485.1:p.Ile4053Lys
XM_011511184.1:c.9998T>A XP_011509486.1:p.Ile3333Lys
NM_004525.3:c.12287T>A MANE Select NP_004516.2:p.Ile4096Lys
XM_011511183.3:c.12158T>A XP_011509485.1:p.Ile4053Lys
XM_011511184.2:c.9998T>A XP_011509486.1:p.Ile3333Lys