Canonical Allele Identifier: CA2661823126

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259348-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259348_169259349insTT , CM000664.2:g.169259348_169259349insTT	GRCh38
NC_000002.11:g.170115858_170115859insTT , CM000664.1:g.170115858_170115859insTT	GRCh37
NC_000002.10:g.169824104_169824105insTT	NCBI36
NG_012634.1:g.108264_108265insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-132_2321-131insAA MANE Select	ENSP00000496870.1:n.2321-132_2321-131insAA
ENST00000263816.7:c.2321-132_2321-131insAA	ENSP00000263816.3:n.2321-132_2321-131insAA
ENST00000443831.1:c.1910-132_1910-131insAA	ENSP00000409813.1:n.1910-132_1910-131insAA
NM_004525.2:c.2321-132_2321-131insAA	NP_004516.2:n.2321-132_2321-131insAA
XM_011511183.1:c.2321-132_2321-131insAA	XP_011509485.1:n.2321-132_2321-131insAA
XM_011511184.1:c.32-132_32-131insAA	XP_011509486.1:n.32-132_32-131insAA
XM_011511185.1:c.2321-132_2321-131insAA	XP_011509487.1:n.2321-132_2321-131insAA
NM_004525.3:c.2321-132_2321-131insAA MANE Select	NP_004516.2:n.2321-132_2321-131insAA
XM_011511183.3:c.2321-132_2321-131insAA	XP_011509485.1:n.2321-132_2321-131insAA
XM_011511184.2:c.32-132_32-131insAA	XP_011509486.1:n.32-132_32-131insAA