Canonical Allele Identifier: CA349158081

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170115565G>T (hg19) ; chr2:g.169259055G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259055G>T , CM000664.2:g.169259055G>T	GRCh38
NC_000002.11:g.170115565G>T , CM000664.1:g.170115565G>T	GRCh37
NC_000002.10:g.169823811G>T	NCBI36
NG_012634.1:g.108558C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2483C>A MANE Select	ENSP00000496870.1:p.Pro828Gln
ENST00000263816.7:c.2483C>A	ENSP00000263816.3:p.Pro828Gln
ENST00000443831.1:c.2072C>A	ENSP00000409813.1:p.Pro691Gln
NM_004525.2:c.2483C>A	NP_004516.2:p.Pro828Gln
XM_011511183.1:c.2483C>A	XP_011509485.1:p.Pro828Gln
XM_011511184.1:c.194C>A	XP_011509486.1:p.Pro65Gln
XM_011511185.1:c.2483C>A	XP_011509487.1:p.Pro828Gln
NM_004525.3:c.2483C>A MANE Select	NP_004516.2:p.Pro828Gln
XM_011511183.3:c.2483C>A	XP_011509485.1:p.Pro828Gln
XM_011511184.2:c.194C>A	XP_011509486.1:p.Pro65Gln