Canonical Allele Identifier: CA349158000

Gene: LRP2

Linked Data

• COSMIC: COSM4382967
• MyVariant Identifiers: chr2:g.170115545G>T (hg19) ; chr2:g.169259035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259035G>T , CM000664.2:g.169259035G>T	GRCh38
NC_000002.11:g.170115545G>T , CM000664.1:g.170115545G>T	GRCh37
NC_000002.10:g.169823791G>T	NCBI36
NG_012634.1:g.108578C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2503C>A MANE Select	ENSP00000496870.1:p.Pro835Thr
ENST00000263816.7:c.2503C>A	ENSP00000263816.3:p.Pro835Thr
ENST00000443831.1:c.2092C>A	ENSP00000409813.1:p.Pro698Thr
NM_004525.2:c.2503C>A	NP_004516.2:p.Pro835Thr
XM_011511183.1:c.2503C>A	XP_011509485.1:p.Pro835Thr
XM_011511184.1:c.214C>A	XP_011509486.1:p.Pro72Thr
XM_011511185.1:c.2503C>A	XP_011509487.1:p.Pro835Thr
NM_004525.3:c.2503C>A MANE Select	NP_004516.2:p.Pro835Thr
XM_011511183.3:c.2503C>A	XP_011509485.1:p.Pro835Thr
XM_011511184.2:c.214C>A	XP_011509486.1:p.Pro72Thr