Canonical Allele Identifier: CA2753102792
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259331C>G , CM000664.2:g.169259331C>G GRCh38
NC_000002.11:g.170115841C>G , CM000664.1:g.170115841C>G GRCh37
NC_000002.10:g.169824087C>G NCBI36
NG_012634.1:g.108282G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-114G>C MANE Select ENSP00000496870.1:n.2321-114G>C
ENST00000263816.7:c.2321-114G>C ENSP00000263816.3:n.2321-114G>C
ENST00000443831.1:c.1910-114G>C ENSP00000409813.1:n.1910-114G>C
NM_004525.2:c.2321-114G>C NP_004516.2:n.2321-114G>C
XM_011511183.1:c.2321-114G>C XP_011509485.1:n.2321-114G>C
XM_011511184.1:c.32-114G>C XP_011509486.1:n.32-114G>C
XM_011511185.1:c.2321-114G>C XP_011509487.1:n.2321-114G>C
NM_004525.3:c.2321-114G>C MANE Select NP_004516.2:n.2321-114G>C
XM_011511183.3:c.2321-114G>C XP_011509485.1:n.2321-114G>C
XM_011511184.2:c.32-114G>C XP_011509486.1:n.32-114G>C