Canonical Allele Identifier: CA1306353811
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259252G= , CM000664.2:g.169259252G= GRCh38
NC_000002.11:g.170115762G= , CM000664.1:g.170115762G= GRCh37
NC_000002.10:g.169824008G= NCBI36
NG_012634.1:g.108361C=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2321-35C= MANE Select ENSP00000496870.1:n.2321-35C=
ENST00000263816.7:c.2321-35C= ENSP00000263816.3:n.2321-35C=
ENST00000443831.1:c.1910-35C= ENSP00000409813.1:n.1910-35C=
NM_004525.2:c.2321-35C= NP_004516.2:n.2321-35C=
XM_011511183.1:c.2321-35C= XP_011509485.1:n.2321-35C=
XM_011511184.1:c.32-35C= XP_011509486.1:n.32-35C=
XM_011511185.1:c.2321-35C= XP_011509487.1:n.2321-35C=
NM_004525.3:c.2321-35C= MANE Select NP_004516.2:n.2321-35C=
XM_011511183.3:c.2321-35C= XP_011509485.1:n.2321-35C=
XM_011511184.2:c.32-35C= XP_011509486.1:n.32-35C=