Canonical Allele Identifier: CA59926732

Gene: LRP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169276576A>G , CM000664.2:g.169276576A>G	GRCh38
NC_000002.11:g.170133086A>G , CM000664.1:g.170133086A>G	GRCh37
NC_000002.10:g.169841332A>G	NCBI36
NG_012634.1:g.91037T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.1772+1169T>C MANE Select	ENSP00000496870.1:n.1772+1169T>C
ENST00000263816.7:c.1772+1169T>C	ENSP00000263816.3:n.1772+1169T>C
ENST00000443831.1:c.1566-1338T>C	ENSP00000409813.1:n.1566-1338T>C
NM_004525.2:c.1772+1169T>C	NP_004516.2:n.1772+1169T>C
XM_011511183.1:c.1772+1169T>C	XP_011509485.1:n.1772+1169T>C
XM_011511185.1:c.1772+1169T>C	XP_011509487.1:n.1772+1169T>C
NM_004525.3:c.1772+1169T>C MANE Select	NP_004516.2:n.1772+1169T>C
XM_011511183.3:c.1772+1169T>C	XP_011509485.1:n.1772+1169T>C