Canonical Allele Identifier: CA59915323
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169177973G>A , CM000664.2:g.169177973G>A GRCh38
NC_000002.11:g.170034483G>A , CM000664.1:g.170034483G>A GRCh37
NC_000002.10:g.169742729G>A NCBI36
NG_012634.1:g.189640C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.10223C>T MANE Select ENSP00000496870.1:p.Pro3408Leu
ENST00000649153.1:c.1123C>T
ENST00000263816.7:c.10223C>T ENSP00000263816.3:p.Pro3408Leu
ENST00000461418.1:n.424C>T
NM_004525.2:c.10223C>T NP_004516.2:p.Pro3408Leu
XM_011511183.1:c.10223C>T XP_011509485.1:p.Pro3408Leu
XM_011511184.1:c.7934C>T XP_011509486.1:p.Pro2645Leu
NM_004525.3:c.10223C>T MANE Select NP_004516.2:p.Pro3408Leu
XM_011511183.3:c.10223C>T XP_011509485.1:p.Pro3408Leu
XM_011511184.2:c.7934C>T XP_011509486.1:p.Pro2645Leu