Canonical Allele Identifier: CA11036936

Gene: LRP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169348336C>T , CM000664.2:g.169348336C>T	GRCh38
NC_000002.11:g.170204846C>T , CM000664.1:g.170204846C>T	GRCh37
NC_000002.10:g.169913092C>T	NCBI36
NG_012634.1:g.19277G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.79+13985G>A MANE Select	ENSP00000496870.1:n.79+13985G>A
ENST00000263816.7:c.79+13985G>A	ENSP00000263816.3:n.79+13985G>A
ENST00000443831.1:c.79+13985G>A	ENSP00000409813.1:n.79+13985G>A
NM_004525.2:c.79+13985G>A	NP_004516.2:n.79+13985G>A
XM_011511183.1:c.79+13985G>A	XP_011509485.1:n.79+13985G>A
XM_011511185.1:c.79+13985G>A	XP_011509487.1:n.79+13985G>A
NM_004525.3:c.79+13985G>A MANE Select	NP_004516.2:n.79+13985G>A
XM_011511183.3:c.79+13985G>A	XP_011509485.1:n.79+13985G>A