Canonical Allele Identifier: CA349152352
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282954T>G , CM000664.2:g.169282954T>G GRCh38
NC_000002.11:g.170139464T>G , CM000664.1:g.170139464T>G GRCh37
NC_000002.10:g.169847710T>G NCBI36
NG_012634.1:g.84659A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.1090A>C MANE Select ENSP00000496870.1:p.Ser364Arg
ENST00000263816.7:c.1090A>C ENSP00000263816.3:p.Ser364Arg
ENST00000443831.1:c.1090A>C ENSP00000409813.1:p.Ser364Arg
NM_004525.2:c.1090A>C NP_004516.2:p.Ser364Arg
XM_011511183.1:c.1090A>C XP_011509485.1:p.Ser364Arg
XM_011511185.1:c.1090A>C XP_011509487.1:p.Ser364Arg
NM_004525.3:c.1090A>C MANE Select NP_004516.2:p.Ser364Arg
XM_011511183.3:c.1090A>C XP_011509485.1:p.Ser364Arg