Canonical Allele Identifier: CA2573133585
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169137376C>T , CM000664.2:g.169137376C>T GRCh38
NC_000002.11:g.169993886C>T , CM000664.1:g.169993886C>T GRCh37
NC_000002.10:g.169702132C>T NCBI36
NG_012634.1:g.230237G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004525.3:c.13620+16G>A MANE Select NP_004516.2:n.13620+16G>A
ENST00000649046.1:c.13620+16G>A MANE Select ENSP00000496870.1:n.13620+16G>A
NM_004525.2:c.13620+16G>A NP_004516.2:n.13620+16G>A
ENST00000263816.7:c.13620+16G>A ENSP00000263816.3:n.13620+16G>A
ENST00000491228.1:n.474+16G>A
ENST00000649153.1:c.4429+16G>A
ENST00000650252.1:c.2611+16G>A ENSP00000496887.1:n.2611+16G>A
XM_011511183.1:c.13491+16G>A XP_011509485.1:n.13491+16G>A
XM_011511183.3:c.13491+16G>A XP_011509485.1:n.13491+16G>A
XM_011511184.1:c.11331+16G>A XP_011509486.1:n.11331+16G>A
XM_011511184.2:c.11331+16G>A XP_011509486.1:n.11331+16G>A