Canonical Allele Identifier: CA1306353814
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259254A= , CM000664.2:g.169259254A= GRCh38
NC_000002.11:g.170115764A= , CM000664.1:g.170115764A= GRCh37
NC_000002.10:g.169824010A= NCBI36
NG_012634.1:g.108359T=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2321-37T= MANE Select ENSP00000496870.1:n.2321-37T=
ENST00000263816.7:c.2321-37T= ENSP00000263816.3:n.2321-37T=
ENST00000443831.1:c.1910-37T= ENSP00000409813.1:n.1910-37T=
NM_004525.2:c.2321-37T= NP_004516.2:n.2321-37T=
XM_011511183.1:c.2321-37T= XP_011509485.1:n.2321-37T=
XM_011511184.1:c.32-37T= XP_011509486.1:n.32-37T=
XM_011511185.1:c.2321-37T= XP_011509487.1:n.2321-37T=
NM_004525.3:c.2321-37T= MANE Select NP_004516.2:n.2321-37T=
XM_011511183.3:c.2321-37T= XP_011509485.1:n.2321-37T=
XM_011511184.2:c.32-37T= XP_011509486.1:n.32-37T=