Canonical Allele Identifier: CA1952854
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs780057389

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154476G>A , CM000664.2:g.169154476G>A GRCh38
NC_000002.11:g.170010986G>A , CM000664.1:g.170010986G>A GRCh37
NC_000002.10:g.169719232G>A NCBI36
NG_012634.1:g.213137C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12279C>T MANE Select ENSP00000496870.1:p.Pro4093=
ENST00000649153.1:c.3179C>T
ENST00000650252.1:c.1307C>T ENSP00000496887.1:p.Pro436Leu
ENST00000263816.7:c.12279C>T ENSP00000263816.3:p.Pro4093=
NM_004525.2:c.12279C>T NP_004516.2:p.Pro4093=
XM_011511183.1:c.12150C>T XP_011509485.1:p.Pro4050=
XM_011511184.1:c.9990C>T XP_011509486.1:p.Pro3330=
NM_004525.3:c.12279C>T MANE Select NP_004516.2:p.Pro4093=
XM_011511183.3:c.12150C>T XP_011509485.1:p.Pro4050=
XM_011511184.2:c.9990C>T XP_011509486.1:p.Pro3330=