Canonical Allele Identifier: CA1306353642

Gene: LRP2

Linked Data

• dbSNP Id: rs1690419495

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169258888_169258891del , CM000664.2:g.169258888_169258891del	GRCh38
NC_000002.11:g.170115398_170115401del , CM000664.1:g.170115398_170115401del	GRCh37
NC_000002.10:g.169823644_169823647del	NCBI36
NG_012634.1:g.108725_108728del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+137_2513+140del MANE Select	ENSP00000496870.1:n.2513+137_2513+140del
ENST00000263816.7:c.2513+137_2513+140del	ENSP00000263816.3:n.2513+137_2513+140del
ENST00000443831.1:c.2102+137_2102+140del	ENSP00000409813.1:n.2102+137_2102+140del
NM_004525.2:c.2513+137_2513+140del	NP_004516.2:n.2513+137_2513+140del
XM_011511183.1:c.2513+137_2513+140del	XP_011509485.1:n.2513+137_2513+140del
XM_011511184.1:c.224+137_224+140del	XP_011509486.1:n.224+137_224+140del
XM_011511185.1:c.2513+137_2513+140del	XP_011509487.1:n.2513+137_2513+140del
NM_004525.3:c.2513+137_2513+140del MANE Select	NP_004516.2:n.2513+137_2513+140del
XM_011511183.3:c.2513+137_2513+140del	XP_011509485.1:n.2513+137_2513+140del
XM_011511184.2:c.224+137_224+140del	XP_011509486.1:n.224+137_224+140del