Canonical Allele Identifier: CA349158489
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259146G>A , CM000664.2:g.169259146G>A GRCh38
NC_000002.11:g.170115656G>A , CM000664.1:g.170115656G>A GRCh37
NC_000002.10:g.169823902G>A NCBI36
NG_012634.1:g.108467C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2392C>T MANE Select ENSP00000496870.1:p.Leu798Phe
ENST00000263816.7:c.2392C>T ENSP00000263816.3:p.Leu798Phe
ENST00000443831.1:c.1981C>T ENSP00000409813.1:p.Leu661Phe
NM_004525.2:c.2392C>T NP_004516.2:p.Leu798Phe
XM_011511183.1:c.2392C>T XP_011509485.1:p.Leu798Phe
XM_011511184.1:c.103C>T XP_011509486.1:p.Leu35Phe
XM_011511185.1:c.2392C>T XP_011509487.1:p.Leu798Phe
NM_004525.3:c.2392C>T MANE Select NP_004516.2:p.Leu798Phe
XM_011511183.3:c.2392C>T XP_011509485.1:p.Leu798Phe
XM_011511184.2:c.103C>T XP_011509486.1:p.Leu35Phe