Canonical Allele Identifier: CA2573049209
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259345_169259347delinsTAA , CM000664.2:g.169259345_169259347delinsTAA GRCh38
NC_000002.11:g.170115855_170115857delinsTAA , CM000664.1:g.170115855_170115857delinsTAA GRCh37
NC_000002.10:g.169824101_169824103delinsTAA NCBI36
NG_012634.1:g.108266_108268delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-130_2321-128delinsTTA MANE Select ENSP00000496870.1:n.2321-130_2321-128delinsTTA
ENST00000263816.7:c.2321-130_2321-128delinsTTA ENSP00000263816.3:n.2321-130_2321-128delinsTTA
ENST00000443831.1:c.1910-130_1910-128delinsTTA ENSP00000409813.1:n.1910-130_1910-128delinsTTA
NM_004525.2:c.2321-130_2321-128delinsTTA NP_004516.2:n.2321-130_2321-128delinsTTA
XM_011511183.1:c.2321-130_2321-128delinsTTA XP_011509485.1:n.2321-130_2321-128delinsTTA
XM_011511184.1:c.32-130_32-128delinsTTA XP_011509486.1:n.32-130_32-128delinsTTA
XM_011511185.1:c.2321-130_2321-128delinsTTA XP_011509487.1:n.2321-130_2321-128delinsTTA
NM_004525.3:c.2321-130_2321-128delinsTTA MANE Select NP_004516.2:n.2321-130_2321-128delinsTTA
XM_011511183.3:c.2321-130_2321-128delinsTTA XP_011509485.1:n.2321-130_2321-128delinsTTA
XM_011511184.2:c.32-130_32-128delinsTTA XP_011509486.1:n.32-130_32-128delinsTTA