Canonical Allele Identifier: CA1306397545
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169348348G= , CM000664.2:g.169348348G= GRCh38
NC_000002.11:g.170204858G= , CM000664.1:g.170204858G= GRCh37
NC_000002.10:g.169913104G= NCBI36
NG_012634.1:g.19265C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.79+13973C= MANE Select ENSP00000496870.1:n.79+13973C=
ENST00000263816.7:c.79+13973C= ENSP00000263816.3:n.79+13973C=
ENST00000443831.1:c.79+13973C= ENSP00000409813.1:n.79+13973C=
NM_004525.2:c.79+13973C= NP_004516.2:n.79+13973C=
XM_011511183.1:c.79+13973C= XP_011509485.1:n.79+13973C=
XM_011511185.1:c.79+13973C= XP_011509487.1:n.79+13973C=
NM_004525.3:c.79+13973C= MANE Select NP_004516.2:n.79+13973C=
XM_011511183.3:c.79+13973C= XP_011509485.1:n.79+13973C=