Canonical Allele Identifier: CA2661822840

Gene: LRP2

Linked Data

• gnomAD v4: 2-169258899-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169258899G>T , CM000664.2:g.169258899G>T	GRCh38
NC_000002.11:g.170115409G>T , CM000664.1:g.170115409G>T	GRCh37
NC_000002.10:g.169823655G>T	NCBI36
NG_012634.1:g.108714C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+126C>A MANE Select	ENSP00000496870.1:n.2513+126C>A
ENST00000263816.7:c.2513+126C>A	ENSP00000263816.3:n.2513+126C>A
ENST00000443831.1:c.2102+126C>A	ENSP00000409813.1:n.2102+126C>A
NM_004525.2:c.2513+126C>A	NP_004516.2:n.2513+126C>A
XM_011511183.1:c.2513+126C>A	XP_011509485.1:n.2513+126C>A
XM_011511184.1:c.224+126C>A	XP_011509486.1:n.224+126C>A
XM_011511185.1:c.2513+126C>A	XP_011509487.1:n.2513+126C>A
NM_004525.3:c.2513+126C>A MANE Select	NP_004516.2:n.2513+126C>A
XM_011511183.3:c.2513+126C>A	XP_011509485.1:n.2513+126C>A
XM_011511184.2:c.224+126C>A	XP_011509486.1:n.224+126C>A