Canonical Allele Identifier: CA59911143

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128798C>T , CM000664.2:g.169128798C>T	GRCh38
NC_000002.11:g.169985308C>T , CM000664.1:g.169985308C>T	GRCh37
NC_000002.10:g.169693554C>T	NCBI36
NG_012634.1:g.238815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13833G>A MANE Select	ENSP00000496870.1:p.Ala4611=
ENST00000649153.1:c.4642G>A
ENST00000650252.1:c.2824G>A	ENSP00000496887.1:n.2824G>A
ENST00000263816.7:c.13833G>A	ENSP00000263816.3:p.Ala4611=
NM_004525.2:c.13833G>A	NP_004516.2:p.Ala4611=
XM_011511183.1:c.13704G>A	XP_011509485.1:p.Ala4568=
XM_011511184.1:c.11544G>A	XP_011509486.1:p.Ala3848=
NM_004525.3:c.13833G>A MANE Select	NP_004516.2:p.Ala4611=
XM_011511183.3:c.13704G>A	XP_011509485.1:p.Ala4568=
XM_011511184.2:c.11544G>A	XP_011509486.1:p.Ala3848=