Canonical Allele Identifier: CA1039047814

Gene: LRP2

Linked Data

• dbSNP Id: rs1686258893
• gnomAD v3: 2-169154438-AG-A
• gnomAD v4: 2-169154438-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154439del , CM000664.2:g.169154439del	GRCh38
NC_000002.11:g.170010949del , CM000664.1:g.170010949del	GRCh37
NC_000002.10:g.169719195del	NCBI36
NG_012634.1:g.213174del

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12295+21del MANE Select	ENSP00000496870.1:n.12295+21del
ENST00000649153.1:c.3195+21del
ENST00000650252.1:c.1323+21del	ENSP00000496887.1:n.1323+21del
ENST00000263816.7:c.12295+21del	ENSP00000263816.3:n.12295+21del
NM_004525.2:c.12295+21del	NP_004516.2:n.12295+21del
XM_011511183.1:c.12166+21del	XP_011509485.1:n.12166+21del
XM_011511184.1:c.10006+21del	XP_011509486.1:n.10006+21del
NM_004525.3:c.12295+21del MANE Select	NP_004516.2:n.12295+21del
XM_011511183.3:c.12166+21del	XP_011509485.1:n.12166+21del
XM_011511184.2:c.10006+21del	XP_011509486.1:n.10006+21del