Canonical Allele Identifier: CA2661822813
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169258873G>T , CM000664.2:g.169258873G>T GRCh38
NC_000002.11:g.170115383G>T , CM000664.1:g.170115383G>T GRCh37
NC_000002.10:g.169823629G>T NCBI36
NG_012634.1:g.108740C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2513+152C>A MANE Select ENSP00000496870.1:n.2513+152C>A
ENST00000263816.7:c.2513+152C>A ENSP00000263816.3:n.2513+152C>A
ENST00000443831.1:c.2102+152C>A ENSP00000409813.1:n.2102+152C>A
NM_004525.2:c.2513+152C>A NP_004516.2:n.2513+152C>A
XM_011511183.1:c.2513+152C>A XP_011509485.1:n.2513+152C>A
XM_011511184.1:c.224+152C>A XP_011509486.1:n.224+152C>A
XM_011511185.1:c.2513+152C>A XP_011509487.1:n.2513+152C>A
NM_004525.3:c.2513+152C>A MANE Select NP_004516.2:n.2513+152C>A
XM_011511183.3:c.2513+152C>A XP_011509485.1:n.2513+152C>A
XM_011511184.2:c.224+152C>A XP_011509486.1:n.224+152C>A