Canonical Allele Identifier: CA1039058130
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1690418998

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169258880A>G , CM000664.2:g.169258880A>G GRCh38
NC_000002.11:g.170115390A>G , CM000664.1:g.170115390A>G GRCh37
NC_000002.10:g.169823636A>G NCBI36
NG_012634.1:g.108733T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2513+145T>C MANE Select ENSP00000496870.1:n.2513+145T>C
ENST00000263816.7:c.2513+145T>C ENSP00000263816.3:n.2513+145T>C
ENST00000443831.1:c.2102+145T>C ENSP00000409813.1:n.2102+145T>C
NM_004525.2:c.2513+145T>C NP_004516.2:n.2513+145T>C
XM_011511183.1:c.2513+145T>C XP_011509485.1:n.2513+145T>C
XM_011511184.1:c.224+145T>C XP_011509486.1:n.224+145T>C
XM_011511185.1:c.2513+145T>C XP_011509487.1:n.2513+145T>C
NM_004525.3:c.2513+145T>C MANE Select NP_004516.2:n.2513+145T>C
XM_011511183.3:c.2513+145T>C XP_011509485.1:n.2513+145T>C
XM_011511184.2:c.224+145T>C XP_011509486.1:n.224+145T>C