Canonical Allele Identifier: CA349158572
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1690433755

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259167A>C , CM000664.2:g.169259167A>C GRCh38
NC_000002.11:g.170115677A>C , CM000664.1:g.170115677A>C GRCh37
NC_000002.10:g.169823923A>C NCBI36
NG_012634.1:g.108446T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2371T>G MANE Select ENSP00000496870.1:p.Phe791Val
ENST00000263816.7:c.2371T>G ENSP00000263816.3:p.Phe791Val
ENST00000443831.1:c.1960T>G ENSP00000409813.1:p.Phe654Val
NM_004525.2:c.2371T>G NP_004516.2:p.Phe791Val
XM_011511183.1:c.2371T>G XP_011509485.1:p.Phe791Val
XM_011511184.1:c.82T>G XP_011509486.1:p.Phe28Val
XM_011511185.1:c.2371T>G XP_011509487.1:p.Phe791Val
NM_004525.3:c.2371T>G MANE Select NP_004516.2:p.Phe791Val
XM_011511183.3:c.2371T>G XP_011509485.1:p.Phe791Val
XM_011511184.2:c.82T>G XP_011509486.1:p.Phe28Val