Canonical Allele Identifier: CA2661822898

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259018-CACTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259021_169259024del , CM000664.2:g.169259021_169259024del	GRCh38
NC_000002.11:g.170115531_170115534del , CM000664.1:g.170115531_170115534del	GRCh37
NC_000002.10:g.169823777_169823780del	NCBI36
NG_012634.1:g.108591_108594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+3_2513+6del MANE Select	ENSP00000496870.1:n.2513+3_2513+6del
ENST00000263816.7:c.2513+3_2513+6del	ENSP00000263816.3:n.2513+3_2513+6del
ENST00000443831.1:c.2102+3_2102+6del	ENSP00000409813.1:n.2102+3_2102+6del
NM_004525.2:c.2513+3_2513+6del	NP_004516.2:n.2513+3_2513+6del
XM_011511183.1:c.2513+3_2513+6del	XP_011509485.1:n.2513+3_2513+6del
XM_011511184.1:c.224+3_224+6del	XP_011509486.1:n.224+3_224+6del
XM_011511185.1:c.2513+3_2513+6del	XP_011509487.1:n.2513+3_2513+6del
NM_004525.3:c.2513+3_2513+6del MANE Select	NP_004516.2:n.2513+3_2513+6del
XM_011511183.3:c.2513+3_2513+6del	XP_011509485.1:n.2513+3_2513+6del
XM_011511184.2:c.224+3_224+6del	XP_011509486.1:n.224+3_224+6del