Canonical Allele Identifier: CA1306353846

Gene: LRP2

Linked Data

• dbSNP Id: rs1690442167

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259319A>G , CM000664.2:g.169259319A>G	GRCh38
NC_000002.11:g.170115829A>G , CM000664.1:g.170115829A>G	GRCh37
NC_000002.10:g.169824075A>G	NCBI36
NG_012634.1:g.108294T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-102T>C MANE Select	ENSP00000496870.1:n.2321-102T>C
ENST00000263816.7:c.2321-102T>C	ENSP00000263816.3:n.2321-102T>C
ENST00000443831.1:c.1910-102T>C	ENSP00000409813.1:n.1910-102T>C
NM_004525.2:c.2321-102T>C	NP_004516.2:n.2321-102T>C
XM_011511183.1:c.2321-102T>C	XP_011509485.1:n.2321-102T>C
XM_011511184.1:c.32-102T>C	XP_011509486.1:n.32-102T>C
XM_011511185.1:c.2321-102T>C	XP_011509487.1:n.2321-102T>C
NM_004525.3:c.2321-102T>C MANE Select	NP_004516.2:n.2321-102T>C
XM_011511183.3:c.2321-102T>C	XP_011509485.1:n.2321-102T>C
XM_011511184.2:c.32-102T>C	XP_011509486.1:n.32-102T>C