Canonical Allele Identifier: CA2661815095

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154356-GCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154360_169154362del , CM000664.2:g.169154360_169154362del	GRCh38
NC_000002.11:g.170010870_170010872del , CM000664.1:g.170010870_170010872del	GRCh37
NC_000002.10:g.169719116_169719118del	NCBI36
NG_012634.1:g.213254_213256del

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12295+101_12295+103del MANE Select	ENSP00000496870.1:n.12295+101_12295+103de...
ENST00000649153.1:c.3195+101_3195+103del
ENST00000650252.1:c.1323+101_1323+103del	ENSP00000496887.1:n.1323+101_1323+103del
ENST00000263816.7:c.12295+101_12295+103del	ENSP00000263816.3:n.12295+101_12295+103de...
NM_004525.2:c.12295+101_12295+103del	NP_004516.2:n.12295+101_12295+103del
XM_011511183.1:c.12166+101_12166+103del	XP_011509485.1:n.12166+101_12166+103del
XM_011511184.1:c.10006+101_10006+103del	XP_011509486.1:n.10006+101_10006+103del
NM_004525.3:c.12295+101_12295+103del MANE Select	NP_004516.2:n.12295+101_12295+103del
XM_011511183.3:c.12166+101_12166+103del	XP_011509485.1:n.12166+101_12166+103del
XM_011511184.2:c.10006+101_10006+103del	XP_011509486.1:n.10006+101_10006+103del