Canonical Allele Identifier: CA349137008

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170010988G>C (hg19) ; chr2:g.169154478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154478G>C , CM000664.2:g.169154478G>C	GRCh38
NC_000002.11:g.170010988G>C , CM000664.1:g.170010988G>C	GRCh37
NC_000002.10:g.169719234G>C	NCBI36
NG_012634.1:g.213135C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12277C>G MANE Select	ENSP00000496870.1:p.Pro4093Ala
ENST00000649153.1:c.3177C>G
ENST00000650252.1:c.1305C>G	ENSP00000496887.1:p.Ile435Met
ENST00000263816.7:c.12277C>G	ENSP00000263816.3:p.Pro4093Ala
NM_004525.2:c.12277C>G	NP_004516.2:p.Pro4093Ala
XM_011511183.1:c.12148C>G	XP_011509485.1:p.Pro4050Ala
XM_011511184.1:c.9988C>G	XP_011509486.1:p.Pro3330Ala
NM_004525.3:c.12277C>G MANE Select	NP_004516.2:p.Pro4093Ala
XM_011511183.3:c.12148C>G	XP_011509485.1:p.Pro4050Ala
XM_011511184.2:c.9988C>G	XP_011509486.1:p.Pro3330Ala