Canonical Allele Identifier: CA2661815071

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154316-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154316A>G , CM000664.2:g.169154316A>G	GRCh38
NC_000002.11:g.170010826A>G , CM000664.1:g.170010826A>G	GRCh37
NC_000002.10:g.169719072A>G	NCBI36
NG_012634.1:g.213297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+144T>C MANE Select	ENSP00000496870.1:n.12295+144T>C
ENST00000649153.1:c.3195+144T>C
ENST00000650252.1:c.1323+144T>C	ENSP00000496887.1:n.1323+144T>C
ENST00000263816.7:c.12295+144T>C	ENSP00000263816.3:n.12295+144T>C
NM_004525.2:c.12295+144T>C	NP_004516.2:n.12295+144T>C
XM_011511183.1:c.12166+144T>C	XP_011509485.1:n.12166+144T>C
XM_011511184.1:c.10006+144T>C	XP_011509486.1:n.10006+144T>C
NM_004525.3:c.12295+144T>C MANE Select	NP_004516.2:n.12295+144T>C
XM_011511183.3:c.12166+144T>C	XP_011509485.1:n.12166+144T>C
XM_011511184.2:c.10006+144T>C	XP_011509486.1:n.10006+144T>C