Canonical Allele Identifier: CA349137050
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154485A>T , CM000664.2:g.169154485A>T GRCh38
NC_000002.11:g.170010995A>T , CM000664.1:g.170010995A>T GRCh37
NC_000002.10:g.169719241A>T NCBI36
NG_012634.1:g.213128T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12270T>A MANE Select ENSP00000496870.1:p.Asp4090Glu
ENST00000649153.1:c.3170T>A
ENST00000650252.1:c.1298T>A ENSP00000496887.1:p.Ile433Asn
ENST00000263816.7:c.12270T>A ENSP00000263816.3:p.Asp4090Glu
NM_004525.2:c.12270T>A NP_004516.2:p.Asp4090Glu
XM_011511183.1:c.12141T>A XP_011509485.1:p.Asp4047Glu
XM_011511184.1:c.9981T>A XP_011509486.1:p.Asp3327Glu
NM_004525.3:c.12270T>A MANE Select NP_004516.2:p.Asp4090Glu
XM_011511183.3:c.12141T>A XP_011509485.1:p.Asp4047Glu
XM_011511184.2:c.9981T>A XP_011509486.1:p.Asp3327Glu