Canonical Allele Identifier: CA2661823029

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259342-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259345del , CM000664.2:g.169259345del	GRCh38
NC_000002.11:g.170115855del , CM000664.1:g.170115855del	GRCh37
NC_000002.10:g.169824101del	NCBI36
NG_012634.1:g.108270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-126del MANE Select	ENSP00000496870.1:n.2321-126del
ENST00000263816.7:c.2321-126del	ENSP00000263816.3:n.2321-126del
ENST00000443831.1:c.1910-126del	ENSP00000409813.1:n.1910-126del
NM_004525.2:c.2321-126del	NP_004516.2:n.2321-126del
XM_011511183.1:c.2321-126del	XP_011509485.1:n.2321-126del
XM_011511184.1:c.32-126del	XP_011509486.1:n.32-126del
XM_011511185.1:c.2321-126del	XP_011509487.1:n.2321-126del
NM_004525.3:c.2321-126del MANE Select	NP_004516.2:n.2321-126del
XM_011511183.3:c.2321-126del	XP_011509485.1:n.2321-126del
XM_011511184.2:c.32-126del	XP_011509486.1:n.32-126del