Canonical Allele Identifier: CA2661815127

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154456-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154458_169154459del , CM000664.2:g.169154458_169154459del	GRCh38
NC_000002.11:g.170010968_170010969del , CM000664.1:g.170010968_170010969del	GRCh37
NC_000002.10:g.169719214_169719215del	NCBI36
NG_012634.1:g.213155_213156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+2_12295+3del MANE Select	ENSP00000496870.1:n.12295+2_12295+3del
ENST00000649153.1:c.3195+2_3195+3del
ENST00000650252.1:c.1323+2_1323+3del	ENSP00000496887.1:n.1323+2_1323+3del
ENST00000263816.7:c.12295+2_12295+3del	ENSP00000263816.3:n.12295+2_12295+3del
NM_004525.2:c.12295+2_12295+3del	NP_004516.2:n.12295+2_12295+3del
XM_011511183.1:c.12166+2_12166+3del	XP_011509485.1:n.12166+2_12166+3del
XM_011511184.1:c.10006+2_10006+3del	XP_011509486.1:n.10006+2_10006+3del
NM_004525.3:c.12295+2_12295+3del MANE Select	NP_004516.2:n.12295+2_12295+3del
XM_011511183.3:c.12166+2_12166+3del	XP_011509485.1:n.12166+2_12166+3del
XM_011511184.2:c.10006+2_10006+3del	XP_011509486.1:n.10006+2_10006+3del