Canonical Allele Identifier: CA59898416
Community Standard Title: NM_004525.3(LRP2):c.12152-295G>C
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154898C>G , CM000664.2:g.169154898C>G GRCh38
NC_000002.11:g.170011408C>G , CM000664.1:g.170011408C>G GRCh37
NC_000002.10:g.169719654C>G NCBI36
NG_012634.1:g.212715G>C

Transcript Alleles

HGVS Amino-acid Change
NM_004525.3:c.12152-295G>C MANE Select NP_004516.2:n.12152-295G>C
ENST00000649046.1:c.12152-295G>C MANE Select ENSP00000496870.1:n.12152-295G>C
NM_004525.2:c.12152-295G>C NP_004516.2:n.12152-295G>C
ENST00000263816.7:c.12152-295G>C ENSP00000263816.3:n.12152-295G>C
ENST00000649153.1:c.3052-295G>C
ENST00000650252.1:c.1184-299G>C ENSP00000496887.1:n.1184-299G>C
XM_011511183.1:c.12023-295G>C XP_011509485.1:n.12023-295G>C
XM_011511183.3:c.12023-295G>C XP_011509485.1:n.12023-295G>C
XM_011511184.1:c.9863-295G>C XP_011509486.1:n.9863-295G>C
XM_011511184.2:c.9863-295G>C XP_011509486.1:n.9863-295G>C